Canonical Allele Identifier: CA2587872995

Gene: C3

Linked Data

• gnomAD v4: 19-6684861-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684861C>T , CM000681.2:g.6684861C>T	GRCh38
NC_000019.9:g.6684872C>T , CM000681.1:g.6684872C>T	GRCh37
NC_000019.8:g.6635872C>T	NCBI36
NG_009557.1:g.40791G>A , LRG_27:g.40791G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2318-27G>A
ENST00000695653.1:c.1879-27G>A	ENSP00000512084.1:n.1879-27G>A
ENST00000695654.1:c.2995-27G>A	ENSP00000512085.1:n.2995-27G>A
ENST00000695690.1:n.161-27G>A
ENST00000695691.1:n.161-27G>A
ENST00000245907.11:c.3970-27G>A MANE Select	ENSP00000245907.4:n.3970-27G>A
ENST00000245907.10:c.3970-27G>A	ENSP00000245907.4:n.3970-27G>A
ENST00000596238.1:n.413-27G>A
ENST00000596548.1:c.52-27G>A	ENSP00000469744.1:n.52-27G>A
ENST00000601008.1:c.241+1885G>A	ENSP00000471384.1:n.241+1885G>A
NM_000064.3:c.3970-27G>A	NP_000055.2:n.3970-27G>A
NM_000064.4:c.3970-27G>A MANE Select	NP_000055.2:n.3970-27G>A