HGVS | Genome Assembly |
---|---|
NC_000019.10:g.12887190C>T , CM000681.2:g.12887190C>T | GRCh38 |
NC_000019.9:g.12998004C>T , CM000681.1:g.12998004C>T | GRCh37 |
NC_000019.8:g.12859004C>T | NCBI36 |
NG_009292.1:g.1031C>T | |
NG_013087.1:g.5014G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264834.6:c.-50G>A MANE Select | ENSP00000264834.3:n.-50G>A | |
NM_006563.3:c.-50G>A | NP_006554.1:n.-50G>A | |
NM_006563.4:c.-50G>A | NP_006554.1:n.-50G>A | |
NM_006563.5:c.-50G>A MANE Select | NP_006554.1:n.-50G>A |