Canonical Allele Identifier: CA2587878388

Gene: C3

Linked Data

• gnomAD v4: 19-6713572-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713572T>C , CM000681.2:g.6713572T>C	GRCh38
NC_000019.9:g.6713583T>C , CM000681.1:g.6713583T>C	GRCh37
NC_000019.8:g.6664583T>C	NCBI36
NG_009557.1:g.12080A>G , LRG_27:g.12080A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-63A>G	ENSP00000512083.1:n.651-63A>G
ENST00000695692.1:n.35A>G
ENST00000245907.11:c.774-63A>G MANE Select	ENSP00000245907.4:n.774-63A>G
ENST00000245907.10:c.774-63A>G	ENSP00000245907.4:n.774-63A>G
ENST00000595577.1:n.278-63A>G
ENST00000597442.5:n.24-63A>G
NM_000064.3:c.774-63A>G	NP_000055.2:n.774-63A>G
NM_000064.4:c.774-63A>G MANE Select	NP_000055.2:n.774-63A>G