HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149928313T>G , CM000663.2:g.149928313T>G | GRCh38 |
NC_000001.10:g.149900205T>G , CM000663.1:g.149900205T>G | GRCh37 |
NC_000001.9:g.148166829T>G | NCBI36 |
NG_032777.1:g.4940A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.8:c.-554A>C | ENSP00000271628.8:n.-554A>C |