Canonical Allele Identifier: CA505192608

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697777G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697766G>C , CM000681.2:g.6697766G>C	GRCh38
NC_000019.9:g.6697777G>C , CM000681.1:g.6697777G>C	GRCh37
NC_000019.8:g.6648777G>C	NCBI36
NG_009557.1:g.27886C>G , LRG_27:g.27886C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.817C>G
ENST00000695652.1:c.2346C>G	ENSP00000512083.1:p.Val782=
ENST00000695653.1:c.378C>G	ENSP00000512084.1:p.Val126=
ENST00000695654.1:c.1593C>G	ENSP00000512085.1:p.Val531=
ENST00000695655.1:c.1410C>G	ENSP00000512086.1:n.1410C>G
ENST00000695692.1:n.1833C>G
ENST00000245907.11:c.2469C>G MANE Select	ENSP00000245907.4:p.Val823=
ENST00000245907.10:c.2469C>G	ENSP00000245907.4:p.Val823=
ENST00000602053.1:n.517C>G
NM_000064.3:c.2469C>G	NP_000055.2:p.Val823=
NM_000064.4:c.2469C>G MANE Select	NP_000055.2:p.Val823=