HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32104885G>C , CM000684.2:g.32104885G>C | GRCh38 |
NC_000022.10:g.32500872G>C , CM000684.1:g.32500872G>C | GRCh37 |
NC_000022.9:g.30830872G>C | NCBI36 |
NG_017045.1:g.66854G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266088.9:c.1765G>C MANE Select | ENSP00000266088.4:p.Glu589Gln | |
ENST00000266088.8:c.1765G>C | ENSP00000266088.4:p.Glu589Gln | |
ENST00000543737.2:c.1384G>C | ENSP00000444898.1:p.Glu462Gln | |
NM_000343.3:c.1765G>C | NP_000334.1:p.Glu589Gln | |
NM_001256314.1:c.1384G>C | NP_001243243.1:p.Glu462Gln | |
XR_938173.1:n.591+1953C>G | ||
XR_938174.1:n.486+14970C>G | ||
NM_000343.4:c.1765G>C MANE Select | NP_000334.1:p.Glu589Gln | |
NM_001256314.2:c.1384G>C | NP_001243243.1:p.Glu462Gln |