HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99321831C>T , CM000666.2:g.99321831C>T | GRCh38 |
NC_000004.11:g.100242988C>T , CM000666.1:g.100242988C>T | GRCh37 |
NC_000004.10:g.100462011C>T | NCBI36 |
NG_011435.1:g.4585G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000639454.1:c.19-2945G>A | ENSP00000491622.1:n.19-2945G>A |