HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39665933C>G , CM000679.2:g.39665933C>G | GRCh38 |
NC_000017.10:g.37822186C>G , CM000679.1:g.37822186C>G | GRCh37 |
NC_000017.9:g.35075712C>G | NCBI36 |
NG_008892.1:g.5588C>G , LRG_210:g.5588C>G | |
NG_042278.1:g.2953C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.3:c.328C>G MANE Select | ENSP00000312624.2:p.Pro110Ala | |
ENST00000309889.2:c.328C>G | ENSP00000312624.2:p.Pro110Ala | |
ENST00000578283.1:c.256C>G | ENSP00000462787.1:p.Pro86Ala | |
NM_003673.3:c.328C>G , LRG_210t1:c.328C>G | NP_003664.1:p.Pro110Ala | |
NM_003673.4:c.328C>G MANE Select | NP_003664.1:p.Pro110Ala |