Canonical Allele Identifier: CA304797283

Gene: C3

Linked Data

• dbSNP Id: rs907261359
• gnomAD v3: 19-6712815-C-G
• gnomAD v4: 19-6712815-C-G
• MyVariant Identifiers: chr19:g.6712826C>G (hg19) ; chr19:g.6712815C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712815C>G , CM000681.2:g.6712815C>G	GRCh38
NC_000019.9:g.6712826C>G , CM000681.1:g.6712826C>G	GRCh37
NC_000019.8:g.6663826C>G	NCBI36
NG_009557.1:g.12837G>C , LRG_27:g.12837G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.881-192G>C	ENSP00000512083.1:n.881-192G>C
ENST00000695654.1:c.128-192G>C	ENSP00000512085.1:n.128-192G>C
ENST00000695692.1:n.328-152G>C
ENST00000245907.11:c.1004-192G>C MANE Select	ENSP00000245907.4:n.1004-192G>C
ENST00000245907.10:c.1004-192G>C	ENSP00000245907.4:n.1004-192G>C
ENST00000594270.5:n.128-213G>C
ENST00000595577.1:n.508-192G>C
ENST00000597442.5:n.254-192G>C
NM_000064.3:c.1004-192G>C	NP_000055.2:n.1004-192G>C
NM_000064.4:c.1004-192G>C MANE Select	NP_000055.2:n.1004-192G>C