HGVS | Genome Assembly |
---|---|
NC_000004.12:g.10041395C= , CM000666.2:g.10041395C= | GRCh38 |
NC_000004.11:g.10043019C= , CM000666.1:g.10043019C= | GRCh37 |
NC_000004.10:g.9652117C= | NCBI36 |
NG_011540.1:g.3854G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506583.5:c.-175-1131G= | ENSP00000422209.1:n.-175-1131G= | |
ENST00000513129.1:c.-41+13438G= | ENSP00000426800.1:n.-41+13438G= |