HGVS | Genome Assembly |
---|---|
NC_000019.10:g.694901G>C , CM000681.2:g.694901G>C | GRCh38 |
NC_000019.9:g.694901G>C , CM000681.1:g.694901G>C | GRCh37 |
NC_000019.8:g.645901G>C | NCBI36 |
NG_051189.1:g.5631C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000329267.9:c.146C>G MANE Select | ENSP00000327386.6:p.Ser49Cys | |
ENST00000329267.8:c.146C>G | ENSP00000327386.6:p.Ser49Cys | |
ENST00000613411.4:c.149C>G | ENSP00000482358.1:p.Ser50Cys | |
NM_001308209.1:c.146C>G | NP_001295138.1:p.Ser49Cys | |
NM_214710.3:c.149C>G | NP_999875.1:p.Ser50Cys | |
NM_214710.4:c.149C>G | NP_999875.1:p.Ser50Cys | |
NM_001308209.2:c.146C>G MANE Select | NP_001295138.2:p.Ser49Cys | |
NM_214710.5:c.149C>G | NP_999875.2:p.Ser50Cys |