HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99321899T>C , CM000666.2:g.99321899T>C | GRCh38 |
NC_000004.11:g.100243056T>C , CM000666.1:g.100243056T>C | GRCh37 |
NC_000004.10:g.100462079T>C | NCBI36 |
NG_011435.1:g.4517A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000639454.1:c.19-3013A>G | ENSP00000491622.1:n.19-3013A>G |