HGVS | Genome Assembly |
---|---|
NC_000011.10:g.62856018A>T , CM000673.2:g.62856018A>T | GRCh38 |
NC_000011.9:g.62623490A>T , CM000673.1:g.62623490A>T | GRCh37 |
NC_000011.8:g.62380066A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680002.1:c.-252A>T | ENSP00000506366.1:n.-252A>T | |
ENST00000680729.1:c.-252A>T | ENSP00000505639.1:n.-252A>T | |
NM_001012662.2:c.-252A>T | NP_001012680.1:n.-252A>T | |
NM_001012664.2:c.-252A>T | NP_001012682.1:n.-252A>T | |
NM_002394.5:c.-252A>T | NP_002385.3:n.-252A>T |