HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24178344T>A , CM000668.2:g.24178344T>A | GRCh38 |
NC_000006.11:g.24178572T>A , CM000668.1:g.24178572T>A | GRCh37 |
NC_000006.10:g.24286551T>A | NCBI36 |
NG_012829.1:g.184709A>T | |
NG_012829.2:g.209949A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.1312A>T MANE Select | ENSP00000367715.3:p.Ser438Cys | |
ENST00000378450.6:c.571A>T | ENSP00000367711.3:p.Ser191Cys | |
ENST00000378454.7:c.1312A>T | ENSP00000367715.3:p.Ser438Cys | |
NM_001195610.1:c.1312A>T | NP_001182539.1:p.Ser438Cys | |
NM_016356.4:c.1312A>T | NP_057440.2:p.Ser438Cys | |
NM_016356.5:c.1312A>T MANE Select | NP_057440.2:p.Ser438Cys | |
NM_001195610.2:c.1312A>T | NP_001182539.1:p.Ser438Cys |