HGVS | Genome Assembly |
---|---|
NC_000003.12:g.139185143G>T , CM000665.2:g.139185143G>T | GRCh38 |
NC_000003.11:g.138903985G>T , CM000665.1:g.138903985G>T | GRCh37 |
NC_000003.10:g.140386675G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000495075.5:c.-72+4783G>T | ENSP00000418008.1:n.-72+4783G>T | |
ENST00000495225.1:c.82+21933G>T | ENSP00000417104.1:n.82+21933G>T |