Canonical Allele Identifier: CA505123729

Gene: C3

Linked Data

• gnomAD v4: 19-6686262-A-G
• MyVariant Identifiers: chr19:g.6686273A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686262A>G , CM000681.2:g.6686262A>G	GRCh38
NC_000019.9:g.6686273A>G , CM000681.1:g.6686273A>G	GRCh37
NC_000019.8:g.6637273A>G	NCBI36
NG_009557.1:g.39390T>C , LRG_27:g.39390T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2020T>C
ENST00000695652.1:c.3549T>C	ENSP00000512083.1:p.Gly1183=
ENST00000695653.1:c.1581T>C	ENSP00000512084.1:p.Gly527=
ENST00000695654.1:c.2697T>C	ENSP00000512085.1:p.Gly899=
ENST00000695655.1:c.2613T>C	ENSP00000512086.1:n.2613T>C
ENST00000695692.1:n.3036T>C
ENST00000245907.11:c.3672T>C MANE Select	ENSP00000245907.4:p.Gly1224=
ENST00000245907.10:c.3672T>C	ENSP00000245907.4:p.Gly1224=
ENST00000596238.1:n.115T>C
ENST00000601008.1:c.241+484T>C	ENSP00000471384.1:n.241+484T>C
NM_000064.3:c.3672T>C	NP_000055.2:p.Gly1224=
NM_000064.4:c.3672T>C MANE Select	NP_000055.2:p.Gly1224=