HGVS | Genome Assembly |
---|---|
NC_000004.12:g.71784863C= , CM000666.2:g.71784863C= | GRCh38 |
NC_000004.11:g.72650580C= , CM000666.1:g.72650580C= | GRCh37 |
NC_000004.10:g.72869444C= | NCBI36 |
NG_012837.2:g.25658G= | |
NG_012837.3:g.25658G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000504199.5:c.22-809G= | ENSP00000421725.1:n.22-809G= | |
ENST00000506245.1:c.-36-809G= | ENSP00000426718.1:n.-36-809G= | |
NM_001204306.1:c.-36-809G= | NP_001191235.1:n.-36-809G= | |
NM_001204307.1:c.22-809G= | NP_001191236.1:n.22-809G= |