HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20618467C>G , CM000663.2:g.20618467C>G | GRCh38 |
NC_000001.10:g.20944960C>G , CM000663.1:g.20944960C>G | GRCh37 |
NC_000001.9:g.20817547C>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375071.4:c.340C>G MANE Select | ENSP00000364212.3:p.Pro114Ala | |
ENST00000375071.3:c.340C>G | ENSP00000364212.3:p.Pro114Ala | |
ENST00000461985.1:n.326C>G | ||
NM_001785.2:c.340C>G | NP_001776.1:p.Pro114Ala | |
NM_001785.3:c.340C>G MANE Select | NP_001776.1:p.Pro114Ala |