Canonical Allele Identifier: CA2587878260

Gene: C3

Linked Data

• gnomAD v4: 19-6713319-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713319A>C , CM000681.2:g.6713319A>C	GRCh38
NC_000019.9:g.6713330A>C , CM000681.1:g.6713330A>C	GRCh37
NC_000019.8:g.6664330A>C	NCBI36
NG_009557.1:g.12333T>G , LRG_27:g.12333T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.754-4T>G	ENSP00000512083.1:n.754-4T>G
ENST00000695692.1:n.201-4T>G
ENST00000245907.11:c.877-4T>G MANE Select	ENSP00000245907.4:n.877-4T>G
ENST00000245907.10:c.877-4T>G	ENSP00000245907.4:n.877-4T>G
ENST00000595577.1:n.381-4T>G
ENST00000597442.5:n.127-4T>G
NM_000064.3:c.877-4T>G	NP_000055.2:n.877-4T>G
NM_000064.4:c.877-4T>G MANE Select	NP_000055.2:n.877-4T>G