Canonical Allele Identifier: CA884148664

Gene: C3

Linked Data

• dbSNP Id: rs1357799511
• gnomAD v3: 19-6709951-C-T
• gnomAD v4: 19-6709951-C-T
• MyVariant Identifiers: chr19:g.6709962C>T (hg19) ; chr19:g.6709951C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709951C>T , CM000681.2:g.6709951C>T	GRCh38
NC_000019.9:g.6709962C>T , CM000681.1:g.6709962C>T	GRCh37
NC_000019.8:g.6660962C>T	NCBI36
NG_009557.1:g.15701G>A , LRG_27:g.15701G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-109G>A	ENSP00000512083.1:n.1564-109G>A
ENST00000695654.1:c.811-109G>A	ENSP00000512085.1:n.811-109G>A
ENST00000695655.1:c.592-73G>A	ENSP00000512086.1:n.592-73G>A
ENST00000695692.1:n.1051-109G>A
ENST00000245907.11:c.1687-109G>A MANE Select	ENSP00000245907.4:n.1687-109G>A
ENST00000245907.10:c.1687-109G>A	ENSP00000245907.4:n.1687-109G>A
ENST00000600763.1:n.320-109G>A
NM_000064.3:c.1687-109G>A	NP_000055.2:n.1687-109G>A
NM_000064.4:c.1687-109G>A MANE Select	NP_000055.2:n.1687-109G>A