HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149928041A>G , CM000663.2:g.149928041A>G | GRCh38 |
NC_000001.10:g.149899933A>G , CM000663.1:g.149899933A>G | GRCh37 |
NC_000001.9:g.148166557A>G | NCBI36 |
NG_032777.1:g.5212T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.8:c.-282T>C | ENSP00000271628.8:n.-282T>C | |
NM_005850.4:c.-282T>C | NP_005841.1:n.-282T>C |