Linked Data
ClinVar Variation Id:
1080387
ClinVar RCV Id:
RCV001395994
dbSNP Id:
rs2153021997
MyVariant Identifiers:
chr4:g.995502C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.1001714C>T , CM000666.2:g.1001714C>T | GRCh38 |
| NC_000004.11:g.995502C>T , CM000666.1:g.995502C>T | GRCh37 |
| NC_000004.10:g.985502C>T | NCBI36 |
| NG_008103.1:g.19718C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000247933.9:c.625C>T | ENSP00000247933.4:p.Leu209= | |
| ENST00000514224.2:c.625C>T MANE Select | ENSP00000425081.2:p.Leu209= | |
| ENST00000652070.1:n.681C>T | ||
| ENST00000247933.8:c.625C>T | ENSP00000247933.4:p.Leu209= | |
| ENST00000502910.5:c.484C>T | ENSP00000422952.1:p.Leu162= | |
| ENST00000504568.5:c.585C>T | ||
| ENST00000509948.5:c.418C>T | ENSP00000424227.1:p.Leu140= | |
| ENST00000514192.5:c.442C>T | ENSP00000423685.1:p.Leu148= | |
| ENST00000514224.1:c.229C>T | ENSP00000425081.1:p.Leu77= | |
| ENST00000514698.5:n.525C>T | ||
| NM_000203.4:c.625C>T | NP_000194.2:p.Leu209= | |
| NR_110313.1:n.713C>T | ||
| XM_006713882.2:c.229C>T | XP_006713945.1:p.Leu77= | |
| XM_011513459.1:c.484C>T | XP_011511761.1:p.Leu162= | |
| XM_011513460.1:c.484C>T | XP_011511762.1:p.Leu162= | |
| XM_011513461.1:c.418C>T | XP_011511763.1:p.Leu140= | |
| XM_011513462.1:c.337C>T | XP_011511764.1:p.Leu113= | |
| XM_011513463.1:c.337C>T | XP_011511765.1:p.Leu113= | |
| XR_924947.1:n.694C>T | ||
| NM_000203.5:c.625C>T MANE Select | NP_000194.2:p.Leu209= | |
| NM_001363576.1:c.229C>T | NP_001350505.1:p.Leu77= | |
| XM_011513461.2:c.418C>T | XP_011511763.1:p.Leu140= | |
| XM_017008163.1:c.-336C>T | XP_016863652.1:n.-336C>T |