Linked Data
ClinVar Variation Id:
2047309
ClinVar RCV Id:
RCV002904209
gnomAD v4:
4-500433-C-T
MyVariant Identifiers:
chr4:g.494222C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.500433C>T , CM000666.2:g.500433C>T | GRCh38 |
| NC_000004.11:g.494222C>T , CM000666.1:g.494222C>T | GRCh37 |
| NC_000004.10:g.484222C>T | NCBI36 |
| NG_051621.1:g.6234C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453061.7:c.192C>T MANE Select | ENSP00000415203.2:p.Leu64= | |
| ENST00000310340.9:c.192C>T | ENSP00000311750.5:p.Leu64= | |
| ENST00000383028.8:c.192C>T | ENSP00000372494.4:p.Leu64= | |
| ENST00000453061.6:c.192C>T | ENSP00000415203.2:p.Leu64= | |
| ENST00000502311.1:n.288C>T | ||
| ENST00000503111.5:c.-76C>T | ENSP00000426002.1:n.-76C>T | |
| ENST00000504187.5:c.192C>T | ENSP00000427069.1:p.Leu64= | |
| ENST00000504346.5:c.-76C>T | ENSP00000424800.1:n.-76C>T | |
| ENST00000506402.5:c.192C>T | ENSP00000424619.1:p.Leu64= | |
| ENST00000509768.1:c.-76C>T | ENSP00000421550.1:n.-76C>T | |
| ENST00000511448.5:c.192C>T | ENSP00000423596.1:p.Leu64= | |
| ENST00000514953.1:n.373-29C>T | ||
| NM_001127178.2:c.192C>T | NP_001120650.1:p.Leu64= | |
| NM_001289051.1:c.-76C>T | NP_001275980.1:n.-76C>T | |
| NM_001289052.1:c.192C>T | NP_001275981.1:p.Leu64= | |
| NM_001289053.1:c.-76C>T | NP_001275982.1:n.-76C>T | |
| NM_001289055.1:c.-245C>T | NP_001275984.1:n.-245C>T | |
| NM_001289057.1:c.-76C>T | NP_001275986.1:n.-76C>T | |
| NM_017733.4:c.192C>T | NP_060203.3:p.Leu64= | |
| NR_110293.1:n.328C>T | ||
| XM_005272283.2:c.192C>T | XP_005272340.1:p.Leu64= | |
| XM_005272284.2:c.-76C>T | XP_005272341.1:n.-76C>T | |
| XM_005272288.3:c.192C>T | XP_005272345.1:p.Leu64= | |
| XM_005272289.2:c.192C>T | XP_005272346.1:p.Leu64= | |
| XM_011513490.1:c.192C>T | XP_011511792.1:p.Leu64= | |
| XM_011513491.1:c.-245C>T | XP_011511793.1:n.-245C>T | |
| XM_011513493.1:c.192C>T | XP_011511795.1:p.Leu64= | |
| XM_011513494.1:c.192C>T | XP_011511796.1:p.Leu64= | |
| XR_924963.1:n.328C>T | ||
| XR_924965.1:n.328C>T | ||
| XR_924966.1:n.328C>T | ||
| XR_924967.1:n.328C>T | ||
| XR_924968.1:n.328C>T | ||
| XR_924969.1:n.328C>T | ||
| XR_924971.1:n.328C>T | ||
| XR_924972.1:n.328C>T | ||
| NM_001345986.1:c.-76C>T | NP_001332915.1:n.-76C>T | |
| NM_001345987.1:c.-76C>T | NP_001332916.1:n.-76C>T | |
| NM_001345988.1:c.-696C>T | NP_001332917.1:n.-696C>T | |
| NM_001345989.1:c.192C>T | NP_001332918.1:p.Leu64= | |
| NM_001345990.1:c.-1434C>T | NP_001332919.1:n.-1434C>T | |
| NM_001345991.1:c.-1296C>T | NP_001332920.1:n.-1296C>T | |
| NM_001345994.1:c.-1021C>T | NP_001332923.1:n.-1021C>T | |
| NR_144326.1:n.564C>T | ||
| NR_144327.1:n.328C>T | ||
| NR_144328.1:n.328C>T | ||
| NR_144329.1:n.564C>T | ||
| NR_144330.1:n.328C>T | ||
| NR_144331.1:n.564C>T | ||
| NR_144332.1:n.328C>T | ||
| NR_144333.1:n.328C>T | ||
| NR_144334.1:n.564C>T | ||
| XM_011513490.3:c.192C>T | XP_011511792.1:p.Leu64= | |
| XM_011513491.2:c.-245C>T | XP_011511793.1:n.-245C>T | |
| XM_011513494.3:c.192C>T | XP_011511796.1:p.Leu64= | |
| XR_001741248.2:n.304C>T | ||
| XR_001741251.2:n.304C>T | ||
| XR_001741253.2:n.304C>T | ||
| XR_001741254.2:n.304C>T | ||
| XR_001741255.2:n.304C>T | ||
| XR_001741258.2:n.304C>T | ||
| XR_001741259.2:n.304C>T | ||
| XR_001741261.2:n.304C>T | ||
| XR_001741262.2:n.304C>T | ||
| XR_002959736.1:n.304C>T | ||
| XR_002959737.1:n.304C>T | ||
| XR_002959738.1:n.304C>T | ||
| XR_924965.3:n.304C>T | ||
| XR_924967.3:n.304C>T | ||
| XR_924969.3:n.304C>T | ||
| XR_924972.3:n.304C>T | ||
| NM_001127178.3:c.192C>T MANE Select | NP_001120650.1:p.Leu64= | |
| NM_001345989.2:c.192C>T | NP_001332918.1:p.Leu64= | |
| NM_001289051.2:c.-76C>T | NP_001275980.1:n.-76C>T | |
| NM_001289052.2:c.192C>T | NP_001275981.1:p.Leu64= | |
| NM_001289053.2:c.-76C>T | NP_001275982.1:n.-76C>T | |
| NM_001289055.2:c.-245C>T | NP_001275984.1:n.-245C>T | |
| NM_001289057.2:c.-76C>T | NP_001275986.1:n.-76C>T | |
| NM_001345986.2:c.-76C>T | NP_001332915.1:n.-76C>T | |
| NM_001345987.2:c.-76C>T | NP_001332916.1:n.-76C>T | |
| NM_001345988.2:c.-696C>T | NP_001332917.1:n.-696C>T | |
| NM_001345990.2:c.-1434C>T | NP_001332919.1:n.-1434C>T | |
| NM_001345991.2:c.-1296C>T | NP_001332920.1:n.-1296C>T | |
| NM_001345994.2:c.-1021C>T | NP_001332923.1:n.-1021C>T | |
| NM_017733.5:c.192C>T | NP_060203.3:p.Leu64= | |
| NR_110293.2:n.318C>T | ||
| NR_144326.2:n.554C>T | ||
| NR_144327.2:n.318C>T | ||
| NR_144328.2:n.318C>T | ||
| NR_144329.2:n.554C>T | ||
| NR_144330.2:n.318C>T | ||
| NR_144331.2:n.554C>T | ||
| NR_144332.2:n.318C>T | ||
| NR_144333.2:n.318C>T | ||
| NR_144334.2:n.554C>T |