HGVS | Genome Assembly |
---|---|
NC_000005.10:g.175443899A>T , CM000667.2:g.175443899A>T | GRCh38 |
NC_000005.9:g.174870902A>T , CM000667.1:g.174870902A>T | GRCh37 |
NC_000005.8:g.174803508A>T | NCBI36 |
NG_011802.1:g.5262T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393752.3:c.-684T>A MANE Select | ENSP00000377353.1:n.-684T>A | |
ENST00000393752.2:c.-684T>A | ENSP00000377353.1:n.-684T>A | |
NM_000794.3:c.-684T>A | NP_000785.1:n.-684T>A | |
NM_000794.4:c.-684T>A | NP_000785.1:n.-684T>A | |
NM_000794.5:c.-684T>A MANE Select | NP_000785.1:n.-684T>A |