Canonical Allele Identifier: CA993064673

Gene: C3

Linked Data

• dbSNP Id: rs1917898865
• gnomAD v3: 19-6682845-T-C
• gnomAD v4: 19-6682845-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682845T>C , CM000681.2:g.6682845T>C	GRCh38
NC_000019.9:g.6682856T>C , CM000681.1:g.6682856T>C	GRCh37
NC_000019.8:g.6633856T>C	NCBI36
NG_009557.1:g.42807A>G , LRG_27:g.42807A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2521-616A>G
ENST00000695653.1:c.2082-616A>G	ENSP00000512084.1:n.2082-616A>G
ENST00000695654.1:c.3198-616A>G	ENSP00000512085.1:n.3198-616A>G
ENST00000695689.1:c.84-179A>G	ENSP00000512101.1:n.84-179A>G
ENST00000695690.1:n.364-616A>G
ENST00000695691.1:n.364-616A>G
ENST00000245907.11:c.4173-616A>G MANE Select	ENSP00000245907.4:n.4173-616A>G
ENST00000245907.10:c.4173-616A>G	ENSP00000245907.4:n.4173-616A>G
ENST00000596548.1:c.294-616A>G	ENSP00000469744.1:n.294-616A>G
ENST00000599899.5:n.516A>G
ENST00000601008.1:c.241+3901A>G	ENSP00000471384.1:n.241+3901A>G
NM_000064.3:c.4173-616A>G	NP_000055.2:n.4173-616A>G
NM_000064.4:c.4173-616A>G MANE Select	NP_000055.2:n.4173-616A>G