Linked Data
ClinVar Variation Id:
390520
dbSNP Id:
rs181746165
ExAC:
6:145948747 G / A
gnomAD v2:
6-145948747-G-A
gnomAD v3:
6-145627611-G-A
gnomAD v4:
6-145627611-G-A
COSMIC:
COSM6038985
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.145627611G>A , CM000668.2:g.145627611G>A | GRCh38 |
| NC_000006.11:g.145948747G>A , CM000668.1:g.145948747G>A | GRCh37 |
| NC_000006.10:g.145990440G>A | NCBI36 |
| NG_012832.1:g.113245C>T | |
| NG_012832.2:g.113245C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367519.9:c.801C>T MANE Select | ENSP00000356489.3:p.Asn267= | |
| ENST00000435470.2:c.801C>T | ENSP00000405913.2:p.Asn267= | |
| ENST00000450221.6:c.340+7634C>T | ENSP00000414900.2:n.340+7634C>T | |
| ENST00000611340.5:c.387C>T | ENSP00000480268.1:p.Asn129= | |
| ENST00000638262.1:c.559C>T | ENSP00000492876.1:p.Arg187Cys | |
| ENST00000638554.1:c.740C>T | ENSP00000492823.1:n.740C>T | |
| ENST00000638597.1:n.258C>T | ||
| ENST00000638717.1:c.501+7634C>T | ||
| ENST00000638778.1:c.387C>T | ENSP00000491353.1:p.Asn129= | |
| ENST00000638783.1:c.387C>T | ENSP00000491338.1:p.Asn129= | |
| ENST00000639049.1:c.1028C>T | ||
| ENST00000639106.1:n.4713C>T | ||
| ENST00000639423.1:c.387C>T | ENSP00000492701.1:p.Asn129= | |
| ENST00000639465.1:c.387C>T | ENSP00000491180.1:p.Asn129= | |
| ENST00000639648.1:n.382C>T | ||
| ENST00000639799.1:n.1342C>T | ||
| ENST00000639859.1:n.6125C>T | ||
| ENST00000640225.1:c.*335C>T | ENSP00000492179.1:n.*335C>T | |
| ENST00000640351.1:c.537C>T | ||
| ENST00000640980.1:c.145C>T | ENSP00000491191.1:p.Arg49Cys | |
| ENST00000367519.7:c.801C>T | ENSP00000356489.3:p.Asn267= | |
| ENST00000435470.1:c.560C>T | ||
| ENST00000450221.5:c.417+7634C>T | ||
| ENST00000611340.4:c.387C>T | ENSP00000480268.1:p.Asn129= | |
| ENST00000618445.4:c.801C>T | ENSP00000480339.1:p.Asn267= | |
| NM_001018041.1:c.801C>T | NP_001018051.1:p.Asn267= | |
| NM_005670.3:c.801C>T | NP_005661.1:p.Asn267= | |
| XM_006715564.2:c.559C>T | XP_006715627.1:p.Arg187Cys | |
| XM_011536113.1:c.718+7634C>T | XP_011534415.1:n.718+7634C>T | |
| XM_011536114.1:c.718+7634C>T | XP_011534416.1:n.718+7634C>T | |
| XM_011536116.1:c.387C>T | XP_011534418.1:p.Asn129= | |
| NM_001360057.1:c.559C>T | NP_001346986.1:p.Arg187Cys | |
| NM_001360064.1:c.387C>T | NP_001346993.1:p.Asn129= | |
| NM_001360071.1:c.387C>T | NP_001347000.1:p.Asn129= | |
| NR_153397.1:n.984C>T | ||
| NR_153398.1:n.372C>T | ||
| XM_011536113.2:c.718+7634C>T | XP_011534415.1:n.718+7634C>T | |
| XM_017011301.1:c.339C>T | XP_016866790.1:p.Asn113= | |
| XM_017011302.1:c.339C>T | XP_016866791.1:p.Asn113= | |
| XM_024446550.1:c.718+7634C>T | XP_024302318.1:n.718+7634C>T | |
| XM_024446551.1:c.387C>T | XP_024302319.1:p.Asn129= | |
| NM_005670.4:c.801C>T MANE Select | NP_005661.1:p.Asn267= | |
| NM_001018041.2:c.801C>T | NP_001018051.1:p.Asn267= | |
| NM_001360057.2:c.559C>T | NP_001346986.1:p.Arg187Cys | |
| NM_001360064.2:c.387C>T | NP_001346993.1:p.Asn129= | |
| NM_001360071.2:c.387C>T | NP_001347000.1:p.Asn129= | |
| NM_001368129.2:c.339C>T | NP_001355058.1:p.Asn113= | |
| NM_001368131.1:c.387C>T | NP_001355060.1:p.Asn129= | |
| NM_001368132.1:c.339C>T | NP_001355061.1:p.Asn113= | |
| NR_153398.2:n.374C>T |