Canonical Allele Identifier: CA2587875505

Gene: C3

Linked Data

• gnomAD v4: 19-6697931-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697931A>C , CM000681.2:g.6697931A>C	GRCh38
NC_000019.9:g.6697942A>C , CM000681.1:g.6697942A>C	GRCh37
NC_000019.8:g.6648942A>C	NCBI36
NG_009557.1:g.27721T>G , LRG_27:g.27721T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-137T>G
ENST00000695652.1:c.2318-137T>G	ENSP00000512083.1:n.2318-137T>G
ENST00000695653.1:c.350-137T>G	ENSP00000512084.1:n.350-137T>G
ENST00000695654.1:c.1565-137T>G	ENSP00000512085.1:n.1565-137T>G
ENST00000695655.1:c.1382-137T>G	ENSP00000512086.1:n.1382-137T>G
ENST00000695692.1:n.1805-137T>G
ENST00000245907.11:c.2441-137T>G MANE Select	ENSP00000245907.4:n.2441-137T>G
ENST00000245907.10:c.2441-137T>G	ENSP00000245907.4:n.2441-137T>G
ENST00000602053.1:n.489-137T>G
NM_000064.3:c.2441-137T>G	NP_000055.2:n.2441-137T>G
NM_000064.4:c.2441-137T>G MANE Select	NP_000055.2:n.2441-137T>G