Canonical Allele Identifier: CA9129767

Gene: C3

Linked Data

• dbSNP Id: rs369109438
• ExAC: 19:6714322 A / G
• gnomAD v2: 19-6714322-A-G
• gnomAD v3: 19-6714311-A-G
• gnomAD v4: 19-6714311-A-G
• MyVariant Identifiers: chr19:g.6714322A>G (hg19) ; chr19:g.6714311A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714311A>G , CM000681.2:g.6714311A>G	GRCh38
NC_000019.9:g.6714322A>G , CM000681.1:g.6714322A>G	GRCh37
NC_000019.8:g.6665322A>G	NCBI36
NG_009557.1:g.11341T>C , LRG_27:g.11341T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.476+41T>C	ENSP00000512083.1:n.476+41T>C
ENST00000245907.11:c.599+41T>C MANE Select	ENSP00000245907.4:n.599+41T>C
ENST00000245907.10:c.599+41T>C	ENSP00000245907.4:n.599+41T>C
ENST00000595577.1:n.41T>C
NM_000064.3:c.599+41T>C	NP_000055.2:n.599+41T>C
NM_000064.4:c.599+41T>C MANE Select	NP_000055.2:n.599+41T>C