HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67583804A>T , CM000673.2:g.67583804A>T | GRCh38 |
NC_000011.9:g.67351275A>T , CM000673.1:g.67351275A>T | GRCh37 |
NC_000011.8:g.67107851A>T | NCBI36 |
NG_012075.1:g.5210A>T , LRG_723:g.5210A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.-40A>T | ENSP00000381604.1:n.-40A>T | |
ENST00000398603.5:c.-40A>T | ENSP00000381604.1:n.-40A>T | |
ENST00000398606.7:c.-40A>T | ENSP00000381607.3:n.-40A>T | |
NM_000852.3:c.-40A>T , LRG_723t1:c.-40A>T | NP_000843.1:n.-40A>T |