MyVariant.info:
GRCh37
chr4:g.47538034C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.47536017C>T , CM000666.2:g.47536017C>T | GRCh38 |
| NC_000004.11:g.47538034C>T , CM000666.1:g.47538034C>T | GRCh37 |
| NC_000004.10:g.47232791C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000273859.8:c.999C>T MANE Select | ENSP00000273859.3:p.Cys333= | |
| ENST00000273859.7:c.999C>T | ENSP00000273859.3:p.Cys333= | |
| ENST00000504445.1:c.999C>T | ENSP00000420909.1:p.Cys333= | |
| NM_020453.3:c.999C>T | NP_065186.3:p.Cys333= | |
| XM_005248119.3:c.999C>T | XP_005248176.1:p.Cys333= | |
| XM_005248120.3:c.999C>T | XP_005248177.1:p.Cys333= | |
| XM_011513722.1:c.804C>T | XP_011512024.1:p.Cys268= | |
| XR_925154.1:n.1285C>T | ||
| XM_005248119.4:c.999C>T | XP_005248176.1:p.Cys333= | |
| XM_005248120.4:c.999C>T | XP_005248177.1:p.Cys333= | |
| XM_011513722.2:c.804C>T | XP_011512024.1:p.Cys268= | |
| XM_017008472.1:c.-587C>T | XP_016863961.1:n.-587C>T | |
| XR_001741295.1:n.1295C>T | ||
| XR_925154.2:n.1281C>T | ||
| NM_020453.4:c.999C>T MANE Select | NP_065186.3:p.Cys333= |