Canonical Allele Identifier: CA505193013

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713243C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713232C>T , CM000681.2:g.6713232C>T	GRCh38
NC_000019.9:g.6713243C>T , CM000681.1:g.6713243C>T	GRCh37
NC_000019.8:g.6664243C>T	NCBI36
NG_009557.1:g.12420G>A , LRG_27:g.12420G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.837G>A	ENSP00000512083.1:p.Val279=
ENST00000695654.1:c.84G>A	ENSP00000512085.1:p.Val28=
ENST00000695692.1:n.284G>A
ENST00000245907.11:c.960G>A MANE Select	ENSP00000245907.4:p.Val320=
ENST00000245907.10:c.960G>A	ENSP00000245907.4:p.Val320=
ENST00000594270.5:n.84G>A
ENST00000595577.1:n.464G>A
ENST00000597442.5:n.210G>A
NM_000064.3:c.960G>A	NP_000055.2:p.Val320=
NM_000064.4:c.960G>A MANE Select	NP_000055.2:p.Val320=