Canonical Allele Identifier: CA2587872294

Gene: C3

Linked Data

• gnomAD v4: 19-6682316-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682316A>C , CM000681.2:g.6682316A>C	GRCh38
NC_000019.9:g.6682327A>C , CM000681.1:g.6682327A>C	GRCh37
NC_000019.8:g.6633327A>C	NCBI36
NG_009557.1:g.43336T>G , LRG_27:g.43336T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2521-87T>G
ENST00000695653.1:c.2082-87T>G	ENSP00000512084.1:n.2082-87T>G
ENST00000695654.1:c.3198-87T>G	ENSP00000512085.1:n.3198-87T>G
ENST00000695689.1:c.144-87T>G	ENSP00000512101.1:n.144-87T>G
ENST00000695690.1:n.364-87T>G
ENST00000695691.1:n.364-87T>G
ENST00000245907.11:c.4173-87T>G MANE Select	ENSP00000245907.4:n.4173-87T>G
ENST00000245907.10:c.4173-87T>G	ENSP00000245907.4:n.4173-87T>G
ENST00000596548.1:c.294-87T>G	ENSP00000469744.1:n.294-87T>G
ENST00000599899.5:n.1045T>G
ENST00000601008.1:c.242-4358T>G	ENSP00000471384.1:n.242-4358T>G
NM_000064.3:c.4173-87T>G	NP_000055.2:n.4173-87T>G
NM_000064.4:c.4173-87T>G MANE Select	NP_000055.2:n.4173-87T>G