HGVS | Genome Assembly |
---|---|
NC_000002.12:g.111712578C>T , CM000664.2:g.111712578C>T | GRCh38 |
NC_000002.11:g.112470155C>T , CM000664.1:g.112470155C>T | GRCh37 |
NC_000002.10:g.112186626C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000643447.1:c.919+17701G>A | ENSP00000494863.1:n.919+17701G>A | |
XM_011512303.1:c.878+1011C>T | XP_011510605.1:n.878+1011C>T |