HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23200717T>A , CM000670.2:g.23200717T>A | GRCh38 |
NC_000008.10:g.23058230T>A , CM000670.1:g.23058230T>A | GRCh37 |
NC_000008.9:g.23114175T>A | NCBI36 |
NG_032107.1:g.29451A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000221132.8:c.673A>T MANE Select | ENSP00000221132.3:p.Ser225Cys | |
ENST00000221132.7:c.673A>T | ENSP00000221132.3:p.Ser225Cys | |
ENST00000524158.5:c.67A>T | ENSP00000428884.1:p.Ser23Cys | |
ENST00000613472.1:c.199A>T | ENSP00000480778.1:p.Ser67Cys | |
NM_003844.3:c.673A>T | NP_003835.3:p.Ser225Cys | |
NM_003844.4:c.673A>T MANE Select | NP_003835.3:p.Ser225Cys |