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