HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149928321G>C , CM000663.2:g.149928321G>C | GRCh38 |
NC_000001.10:g.149900213G>C , CM000663.1:g.149900213G>C | GRCh37 |
NC_000001.9:g.148166837G>C | NCBI36 |
NG_032777.1:g.4932C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.8:c.-562C>G | ENSP00000271628.8:n.-562C>G |