HGVS | Genome Assembly |
---|---|
NC_000012.12:g.47910677C>A , CM000674.2:g.47910677C>A | GRCh38 |
NC_000012.11:g.48304460C>A , CM000674.1:g.48304460C>A | GRCh37 |
NC_000012.10:g.46590727C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395324.6:c.-83-27903G>T | ENSP00000378734.2:n.-83-27903G>T |