HGVS | Genome Assembly |
---|---|
NC_000009.12:g.120927879C>T , CM000671.2:g.120927879C>T | GRCh38 |
NC_000009.11:g.123690157C>T , CM000671.1:g.123690157C>T | GRCh37 |
NC_000009.10:g.122729978C>T | NCBI36 |
NG_023346.1:g.6295G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373887.7:c.-1556G>A | ENSP00000362994.3:n.-1556G>A | |
ENST00000540010.1:c.-365-1191G>A | ENSP00000443183.1:n.-365-1191G>A | |
NM_001190945.1:c.-365-1191G>A | NP_001177874.1:n.-365-1191G>A | |
NM_001190945.2:c.-365-1191G>A | NP_001177874.1:n.-365-1191G>A |