Canonical Allele Identifier: CA505123672

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686177G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686166G>C , CM000681.2:g.6686166G>C	GRCh38
NC_000019.9:g.6686177G>C , CM000681.1:g.6686177G>C	GRCh37
NC_000019.8:g.6637177G>C	NCBI36
NG_009557.1:g.39486C>G , LRG_27:g.39486C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2116C>G
ENST00000695652.1:c.3645C>G	ENSP00000512083.1:p.Leu1215=
ENST00000695653.1:c.1677C>G	ENSP00000512084.1:p.Leu559=
ENST00000695654.1:c.2793C>G	ENSP00000512085.1:p.Leu931=
ENST00000695655.1:c.2709C>G	ENSP00000512086.1:n.2709C>G
ENST00000695692.1:n.3132C>G
ENST00000245907.11:c.3768C>G MANE Select	ENSP00000245907.4:p.Leu1256=
ENST00000245907.10:c.3768C>G	ENSP00000245907.4:p.Leu1256=
ENST00000596238.1:n.211C>G
ENST00000601008.1:c.241+580C>G	ENSP00000471384.1:n.241+580C>G
NM_000064.3:c.3768C>G	NP_000055.2:p.Leu1256=
NM_000064.4:c.3768C>G MANE Select	NP_000055.2:p.Leu1256=