Linked Data
ClinVar Variation Id:
472941
dbSNP Id:
rs148923187
ExAC:
7:2579497 G / A
gnomAD v2:
7-2579497-G-A
gnomAD v3:
7-2539863-G-A
gnomAD v4:
7-2539863-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.2539863G>A , CM000669.2:g.2539863G>A | GRCh38 |
| NC_000007.13:g.2579497G>A , CM000669.1:g.2579497G>A | GRCh37 |
| NC_000007.12:g.2546023G>A | NCBI36 |
| NG_032167.1:g.20896C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340611.9:c.1421C>T MANE Select | ENSP00000339637.4:p.Thr474Met | |
| ENST00000340611.8:c.1421C>T | ENSP00000339637.4:p.Thr474Met | |
| ENST00000467558.5:n.2793C>T | ||
| ENST00000469750.5:n.3993C>T | ||
| ENST00000473879.1:n.137C>T | ||
| ENST00000493232.5:n.4157C>T | ||
| NM_152743.3:c.1421C>T | NP_689956.2:p.Thr474Met | |
| XM_005249643.3:c.1421C>T | XP_005249700.1:p.Thr474Met | |
| XM_011515177.1:c.1505C>T | XP_011513479.1:p.Thr502Met | |
| XM_011515178.1:c.1505C>T | XP_011513480.1:p.Thr502Met | |
| XM_011515179.1:c.1502C>T | XP_011513481.1:p.Thr501Met | |
| XM_011515180.1:c.1475C>T | XP_011513482.1:p.Thr492Met | |
| XM_011515181.1:c.1505C>T | XP_011513483.1:p.Thr502Met | |
| XM_011515182.1:c.1505C>T | XP_011513484.1:p.Thr502Met | |
| XM_011515183.1:c.980C>T | XP_011513485.1:p.Thr327Met | |
| XM_011515184.1:c.980C>T | XP_011513486.1:p.Thr327Met | |
| XM_011515185.1:c.1421C>T | XP_011513487.1:p.Thr474Met | |
| XM_011515186.1:c.1505C>T | XP_011513488.1:p.Thr502Met | |
| XM_011515187.1:c.77C>T | XP_011513489.1:p.Thr26Met | |
| NM_001350626.1:c.1421C>T | NP_001337555.1:p.Thr474Met | |
| NM_001350627.1:c.896C>T | NP_001337556.1:p.Thr299Met | |
| NR_146879.1:n.1838C>T | ||
| XM_011515177.2:c.1505C>T | XP_011513479.1:p.Thr502Met | |
| XM_011515179.2:c.1502C>T | XP_011513481.1:p.Thr501Met | |
| XM_011515181.2:c.1505C>T | XP_011513483.1:p.Thr502Met | |
| XM_011515182.2:c.1505C>T | XP_011513484.1:p.Thr502Met | |
| XM_011515184.3:c.980C>T | XP_011513486.1:p.Thr327Met | |
| XM_011515186.2:c.1505C>T | XP_011513488.1:p.Thr502Met | |
| XM_017011833.1:c.1418C>T | XP_016867322.1:p.Thr473Met | |
| XM_017011834.1:c.1418C>T | XP_016867323.1:p.Thr473Met | |
| XM_017011836.2:c.1421C>T | XP_016867325.1:p.Thr474Met | |
| XM_024446682.1:c.77C>T | XP_024302450.1:p.Thr26Met | |
| NM_152743.4:c.1421C>T MANE Select | NP_689956.2:p.Thr474Met | |
| NM_001350626.2:c.1421C>T | NP_001337555.1:p.Thr474Met | |
| NM_001350627.2:c.896C>T | NP_001337556.1:p.Thr299Met | |
| NR_146879.2:n.1604C>T |