Canonical Allele Identifier: CA9129718

Gene: C3

Linked Data

• dbSNP Id: rs186166756
• ExAC: 19:6714122 G / A
• gnomAD v2: 19-6714122-G-A
• gnomAD v3: 19-6714111-G-A
• gnomAD v4: 19-6714111-G-A
• MyVariant Identifiers: chr19:g.6714122G>A (hg19) ; chr19:g.6714111G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714111G>A , CM000681.2:g.6714111G>A	GRCh38
NC_000019.9:g.6714122G>A , CM000681.1:g.6714122G>A	GRCh37
NC_000019.8:g.6665122G>A	NCBI36
NG_009557.1:g.11541C>T , LRG_27:g.11541C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.560-29C>T	ENSP00000512083.1:n.560-29C>T
ENST00000245907.11:c.683-29C>T MANE Select	ENSP00000245907.4:n.683-29C>T
ENST00000245907.10:c.683-29C>T	ENSP00000245907.4:n.683-29C>T
ENST00000595577.1:n.187-29C>T
NM_000064.3:c.683-29C>T	NP_000055.2:n.683-29C>T
NM_000064.4:c.683-29C>T MANE Select	NP_000055.2:n.683-29C>T