HGVS | Genome Assembly |
---|---|
NC_000009.12:g.120927961G>A , CM000671.2:g.120927961G>A | GRCh38 |
NC_000009.11:g.123690239G>A , CM000671.1:g.123690239G>A | GRCh37 |
NC_000009.10:g.122730060G>A | NCBI36 |
NG_023346.1:g.6213C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000373887.7:c.-1638C>T | ENSP00000362994.3:n.-1638C>T | |
ENST00000540010.1:c.-366+1153C>T | ENSP00000443183.1:n.-366+1153C>T | |
NM_001190945.1:c.-366+1153C>T | NP_001177874.1:n.-366+1153C>T | |
NM_001190945.2:c.-366+1153C>T | NP_001177874.1:n.-366+1153C>T |