HGVS | Genome Assembly |
---|---|
NC_000001.11:g.58576739C>G , CM000663.2:g.58576739C>G | GRCh38 |
NC_000001.10:g.59042411C>G , CM000663.1:g.59042411C>G | GRCh37 |
NC_000001.9:g.58814999C>G | NCBI36 |
NG_016237.1:g.5756G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371225.4:c.418G>C MANE Select | ENSP00000360269.2:p.Asp140His | |
ENST00000371225.3:c.418G>C | ENSP00000360269.2:p.Asp140His | |
NM_002353.2:c.418G>C | NP_002344.2:p.Asp140His | |
NM_002353.3:c.418G>C MANE Select | NP_002344.2:p.Asp140His |