HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461635G>A , CM000672.2:g.122461635G>A | GRCh38 |
NC_000010.10:g.124221151G>A , CM000672.1:g.124221151G>A | GRCh37 |
NC_000010.9:g.124211141G>A | NCBI36 |
NG_011554.1:g.5111G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.-18G>A MANE Select | ENSP00000357980.3:n.-18G>A | |
ENST00000648167.1:c.154+2926G>A | ENSP00000498033.1:n.154+2926G>A | |
ENST00000368984.7:c.-18G>A | ENSP00000357980.3:n.-18G>A | |
NM_002775.4:c.-18G>A | NP_002766.1:n.-18G>A | |
NM_002775.5:c.-18G>A MANE Select | NP_002766.1:n.-18G>A |