HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442487T>C , CM000666.2:g.177442487T>C | GRCh38 |
NC_000004.11:g.178363641T>C , CM000666.1:g.178363641T>C | GRCh37 |
NC_000004.10:g.178600635T>C | NCBI36 |
NG_011845.2:g.5017A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264595.6:c.-112A>G | ENSP00000264595.2:n.-112A>G | |
NM_000027.3:c.-112A>G | NP_000018.2:n.-112A>G | |
NM_001171988.1:c.-112A>G | NP_001165459.1:n.-112A>G | |
NR_033655.1:n.17A>G | ||
XM_006714123.2:c.-112A>G | XP_006714186.1:n.-112A>G |