HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102725749A>C , CM000673.2:g.102725749A>C | GRCh38 |
NC_000011.9:g.102596480A>C , CM000673.1:g.102596480A>C | GRCh37 |
NC_000011.8:g.102101690A>C | NCBI36 |
NG_012101.1:g.4206T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000528662.6:c.-148-746T>G | ENSP00000431431.2:n.-148-746T>G |