Canonical Allele Identifier: CA403619329
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6686125T>C , CM000681.2:g.6686125T>C GRCh38
NC_000019.9:g.6686136T>C , CM000681.1:g.6686136T>C GRCh37
NC_000019.8:g.6637136T>C NCBI36
NG_009557.1:g.39527A>G , LRG_27:g.39527A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2157A>G
ENST00000695652.1:c.3686A>G ENSP00000512083.1:p.Gln1229Arg
ENST00000695653.1:c.1718A>G ENSP00000512084.1:p.Gln573Arg
ENST00000695654.1:c.2834A>G ENSP00000512085.1:p.Gln945Arg
ENST00000695655.1:c.2750A>G ENSP00000512086.1:n.2750A>G
ENST00000695692.1:n.3173A>G
ENST00000245907.11:c.3809A>G MANE Select ENSP00000245907.4:p.Gln1270Arg
ENST00000245907.10:c.3809A>G ENSP00000245907.4:p.Gln1270Arg
ENST00000596238.1:n.252A>G
ENST00000601008.1:c.241+621A>G ENSP00000471384.1:n.241+621A>G
NM_000064.3:c.3809A>G NP_000055.2:p.Gln1270Arg
NM_000064.4:c.3809A>G MANE Select NP_000055.2:p.Gln1270Arg