gnomAD v2:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.127614497G>T , CM000669.2:g.127614497G>T | GRCh38 |
| NC_000007.13:g.127254551G>T , CM000669.1:g.127254551G>T | GRCh37 |
| NC_000007.12:g.127041787G>T | NCBI36 |
| NG_012848.1:g.6230C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000639438.3:c.421C>A MANE Select | ENSP00000491782.1:p.Arg141= | |
| ENST00000338516.7:c.421C>A | ENSP00000344297.4:p.Arg141= | |
| ENST00000341640.6:c.397C>A | ENSP00000339906.2:p.Arg133= | |
| ENST00000378740.6:c.397C>A | ENSP00000368014.3:p.Arg133= | |
| ENST00000463946.5:c.391C>A | ENSP00000451923.1:p.Arg131= | |
| ENST00000477423.1:n.391C>A | ||
| ENST00000483494.5:c.391C>A | ENSP00000473846.1:p.Arg131= | |
| ENST00000611453.1:c.391C>A | ENSP00000477877.1:p.Arg131= | |
| NM_006193.2:c.397C>A | NP_006184.2:p.Arg133= | |
| XM_011516276.1:c.421C>A | XP_011514578.1:p.Arg141= | |
| NM_001366110.1:c.421C>A MANE Select | NP_001353039.1:p.Arg141= | |
| NM_001366111.1:c.421C>A | NP_001353040.1:p.Arg141= |