Canonical Allele Identifier: CA505124813

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709812T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709801T>C , CM000681.2:g.6709801T>C	GRCh38
NC_000019.9:g.6709812T>C , CM000681.1:g.6709812T>C	GRCh37
NC_000019.8:g.6660812T>C	NCBI36
NG_009557.1:g.15851A>G , LRG_27:g.15851A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1605A>G	ENSP00000512083.1:p.Val535=
ENST00000695654.1:c.852A>G	ENSP00000512085.1:p.Val284=
ENST00000695655.1:c.669A>G	ENSP00000512086.1:n.669A>G
ENST00000695692.1:n.1092A>G
ENST00000245907.11:c.1728A>G MANE Select	ENSP00000245907.4:p.Val576=
ENST00000245907.10:c.1728A>G	ENSP00000245907.4:p.Val576=
ENST00000600763.1:n.361A>G
NM_000064.3:c.1728A>G	NP_000055.2:p.Val576=
NM_000064.4:c.1728A>G MANE Select	NP_000055.2:p.Val576=