HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44456618G>A , CM000683.2:g.44456618G>A | GRCh38 |
NC_000021.8:g.45876501G>A , CM000683.1:g.45876501G>A | GRCh37 |
NC_000021.7:g.44700929G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291592.6:c.-27G>A MANE Select | ENSP00000291592.4:n.-27G>A | |
ENST00000291592.5:c.-27G>A | ENSP00000291592.4:n.-27G>A | |
NM_030891.4:c.-27G>A | NP_112153.1:n.-27G>A | |
NM_030891.5:c.-27G>A | NP_112153.1:n.-27G>A | |
NM_030891.6:c.-27G>A MANE Select | NP_112153.1:n.-27G>A |