HGVS | Genome Assembly |
---|---|
NC_000002.12:g.27323120C>T , CM000664.2:g.27323120C>T | GRCh38 |
NC_000002.11:g.27545987C>T , CM000664.1:g.27545987C>T | GRCh37 |
NC_000002.10:g.27399491C>T | NCBI36 |
NG_008075.1:g.4445G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357186.10:c.18+1313G>A | ENSP00000349713.6:n.18+1313G>A | |
XM_005264327.2:c.-198G>A | XP_005264384.1:n.-198G>A |