HGVS | Genome Assembly |
---|---|
NC_000011.10:g.1100043G>T , CM000673.2:g.1100043G>T | GRCh38 |
NC_000011.9:g.1093951G>T , CM000673.1:g.1093951G>T | GRCh37 |
NC_000011.8:g.1083951G>T | NCBI36 |
NG_051929.1:g.32070G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000361558.7:n.9809+18G>T | ||
ENST00000674892.1:c.256+18G>T | ENSP00000501871.1:n.256+18G>T |