Canonical Allele Identifier: CA505193121

Gene: C3

Linked Data

• dbSNP Id: rs2145430774
• MyVariant Identifiers: chr19:g.6713309C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713298C>T , CM000681.2:g.6713298C>T	GRCh38
NC_000019.9:g.6713309C>T , CM000681.1:g.6713309C>T	GRCh37
NC_000019.8:g.6664309C>T	NCBI36
NG_009557.1:g.12354G>A , LRG_27:g.12354G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.771G>A	ENSP00000512083.1:p.Gly257=
ENST00000695654.1:c.18G>A	ENSP00000512085.1:p.Gly6=
ENST00000695692.1:n.218G>A
ENST00000245907.11:c.894G>A MANE Select	ENSP00000245907.4:p.Gly298=
ENST00000245907.10:c.894G>A	ENSP00000245907.4:p.Gly298=
ENST00000594270.5:n.18G>A
ENST00000595577.1:n.398G>A
ENST00000597442.5:n.144G>A
NM_000064.3:c.894G>A	NP_000055.2:p.Gly298=
NM_000064.4:c.894G>A MANE Select	NP_000055.2:p.Gly298=