Canonical Allele Identifier: CA403643017
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714054C>G , CM000681.2:g.6714054C>G GRCh38
NC_000019.9:g.6714065C>G , CM000681.1:g.6714065C>G GRCh37
NC_000019.8:g.6665065C>G NCBI36
NG_009557.1:g.11598G>C , LRG_27:g.11598G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.588G>C ENSP00000512083.1:p.Glu196Asp
ENST00000245907.11:c.711G>C MANE Select ENSP00000245907.4:p.Glu237Asp
ENST00000245907.10:c.711G>C ENSP00000245907.4:p.Glu237Asp
ENST00000595577.1:n.215G>C
NM_000064.3:c.711G>C NP_000055.2:p.Glu237Asp
NM_000064.4:c.711G>C MANE Select NP_000055.2:p.Glu237Asp