Canonical Allele Identifier: CA2587873347

Gene: C3

Linked Data

• gnomAD v4: 19-6686000-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686000G>T , CM000681.2:g.6686000G>T	GRCh38
NC_000019.9:g.6686011G>T , CM000681.1:g.6686011G>T	GRCh37
NC_000019.8:g.6637011G>T	NCBI36
NG_009557.1:g.39652C>A , LRG_27:g.39652C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2158+124C>A
ENST00000695653.1:c.1719+124C>A	ENSP00000512084.1:n.1719+124C>A
ENST00000695654.1:c.2835+124C>A	ENSP00000512085.1:n.2835+124C>A
ENST00000245907.11:c.3810+124C>A MANE Select	ENSP00000245907.4:n.3810+124C>A
ENST00000245907.10:c.3810+124C>A	ENSP00000245907.4:n.3810+124C>A
ENST00000596238.1:n.253+124C>A
ENST00000601008.1:c.241+746C>A	ENSP00000471384.1:n.241+746C>A
NM_000064.3:c.3810+124C>A	NP_000055.2:n.3810+124C>A
NM_000064.4:c.3810+124C>A MANE Select	NP_000055.2:n.3810+124C>A