Canonical Allele Identifier: CA505193186

Gene: C3

Linked Data

• COSMIC: COSM1613049
• MyVariant Identifiers: chr19:g.6713520C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713509C>T , CM000681.2:g.6713509C>T	GRCh38
NC_000019.9:g.6713520C>T , CM000681.1:g.6713520C>T	GRCh37
NC_000019.8:g.6664520C>T	NCBI36
NG_009557.1:g.12143G>A , LRG_27:g.12143G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651G>A	ENSP00000512083.1:p.Arg217=
ENST00000695692.1:n.98G>A
ENST00000245907.11:c.774G>A MANE Select	ENSP00000245907.4:p.Arg258=
ENST00000245907.10:c.774G>A	ENSP00000245907.4:p.Arg258=
ENST00000595577.1:n.278G>A
ENST00000597442.5:n.24G>A
NM_000064.3:c.774G>A	NP_000055.2:p.Arg258=
NM_000064.4:c.774G>A MANE Select	NP_000055.2:p.Arg258=