Canonical Allele Identifier: CA403642324

Gene: C3

Linked Data

• COSMIC: COSM4836800
• MyVariant Identifiers: chr19:g.6713311C>A (hg19) ; chr19:g.6713300C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713300C>A , CM000681.2:g.6713300C>A	GRCh38
NC_000019.9:g.6713311C>A , CM000681.1:g.6713311C>A	GRCh37
NC_000019.8:g.6664311C>A	NCBI36
NG_009557.1:g.12352G>T , LRG_27:g.12352G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.769G>T	ENSP00000512083.1:p.Gly257Trp
ENST00000695654.1:c.16G>T	ENSP00000512085.1:p.Gly6Trp
ENST00000695692.1:n.216G>T
ENST00000245907.11:c.892G>T MANE Select	ENSP00000245907.4:p.Gly298Trp
ENST00000245907.10:c.892G>T	ENSP00000245907.4:p.Gly298Trp
ENST00000594270.5:n.16G>T
ENST00000595577.1:n.396G>T
ENST00000597442.5:n.142G>T
NM_000064.3:c.892G>T	NP_000055.2:p.Gly298Trp
NM_000064.4:c.892G>T MANE Select	NP_000055.2:p.Gly298Trp