HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461632G>C , CM000672.2:g.122461632G>C | GRCh38 |
NC_000010.10:g.124221148G>C , CM000672.1:g.124221148G>C | GRCh37 |
NC_000010.9:g.124211138G>C | NCBI36 |
NG_011554.1:g.5108G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.-21G>C MANE Select | ENSP00000357980.3:n.-21G>C | |
ENST00000648167.1:c.154+2923G>C | ENSP00000498033.1:n.154+2923G>C | |
ENST00000368984.7:c.-21G>C | ENSP00000357980.3:n.-21G>C | |
NM_002775.4:c.-21G>C | NP_002766.1:n.-21G>C | |
NM_002775.5:c.-21G>C MANE Select | NP_002766.1:n.-21G>C |