Canonical Allele Identifier: CA2587878186

Gene: C3

Linked Data

• gnomAD v4: 19-6713087-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713087T>C , CM000681.2:g.6713087T>C	GRCh38
NC_000019.9:g.6713098T>C , CM000681.1:g.6713098T>C	GRCh37
NC_000019.8:g.6664098T>C	NCBI36
NG_009557.1:g.12565A>G , LRG_27:g.12565A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.880+102A>G	ENSP00000512083.1:n.880+102A>G
ENST00000695654.1:c.127+102A>G	ENSP00000512085.1:n.127+102A>G
ENST00000695692.1:n.327+102A>G
ENST00000245907.11:c.1003+102A>G MANE Select	ENSP00000245907.4:n.1003+102A>G
ENST00000245907.10:c.1003+102A>G	ENSP00000245907.4:n.1003+102A>G
ENST00000594270.5:n.127+102A>G
ENST00000595577.1:n.507+102A>G
ENST00000597442.5:n.253+102A>G
NM_000064.3:c.1003+102A>G	NP_000055.2:n.1003+102A>G
NM_000064.4:c.1003+102A>G MANE Select	NP_000055.2:n.1003+102A>G