Canonical Allele Identifier: CA403642580

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713459C>G (hg19) ; chr19:g.6713448C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713448C>G , CM000681.2:g.6713448C>G	GRCh38
NC_000019.9:g.6713459C>G , CM000681.1:g.6713459C>G	GRCh37
NC_000019.8:g.6664459C>G	NCBI36
NG_009557.1:g.12204G>C , LRG_27:g.12204G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.712G>C	ENSP00000512083.1:p.Glu238Gln
ENST00000695692.1:n.159G>C
ENST00000245907.11:c.835G>C MANE Select	ENSP00000245907.4:p.Glu279Gln
ENST00000245907.10:c.835G>C	ENSP00000245907.4:p.Glu279Gln
ENST00000595577.1:n.339G>C
ENST00000597442.5:n.85G>C
NM_000064.3:c.835G>C	NP_000055.2:p.Glu279Gln
NM_000064.4:c.835G>C MANE Select	NP_000055.2:p.Glu279Gln