HGVS | Genome Assembly |
---|---|
NC_000004.12:g.107193985T>C , CM000666.2:g.107193985T>C | GRCh38 |
NC_000004.11:g.108115142T>C , CM000666.1:g.108115142T>C | GRCh37 |
NC_000004.10:g.108334591T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000510463.1:c.-83-5460A>G | ENSP00000423797.1:n.-83-5460A>G | |
ENST00000513208.5:c.-177-5460A>G | ENSP00000421255.1:n.-177-5460A>G |