Canonical Allele Identifier: CA403642572

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713457T>A (hg19) ; chr19:g.6713446T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713446T>A , CM000681.2:g.6713446T>A	GRCh38
NC_000019.9:g.6713457T>A , CM000681.1:g.6713457T>A	GRCh37
NC_000019.8:g.6664457T>A	NCBI36
NG_009557.1:g.12206A>T , LRG_27:g.12206A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.714A>T	ENSP00000512083.1:p.Glu238Asp
ENST00000695692.1:n.161A>T
ENST00000245907.11:c.837A>T MANE Select	ENSP00000245907.4:p.Glu279Asp
ENST00000245907.10:c.837A>T	ENSP00000245907.4:p.Glu279Asp
ENST00000595577.1:n.341A>T
ENST00000597442.5:n.87A>T
NM_000064.3:c.837A>T	NP_000055.2:p.Glu279Asp
NM_000064.4:c.837A>T MANE Select	NP_000055.2:p.Glu279Asp