Canonical Allele Identifier: CA403642360

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713320C>T (hg19) ; chr19:g.6713309C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713309C>T , CM000681.2:g.6713309C>T	GRCh38
NC_000019.9:g.6713320C>T , CM000681.1:g.6713320C>T	GRCh37
NC_000019.8:g.6664320C>T	NCBI36
NG_009557.1:g.12343G>A , LRG_27:g.12343G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.760G>A	ENSP00000512083.1:p.Asp254Asn
ENST00000695654.1:c.7G>A	ENSP00000512085.1:p.Asp3Asn
ENST00000695692.1:n.207G>A
ENST00000245907.11:c.883G>A MANE Select	ENSP00000245907.4:p.Asp295Asn
ENST00000245907.10:c.883G>A	ENSP00000245907.4:p.Asp295Asn
ENST00000594270.5:n.7G>A
ENST00000595577.1:n.387G>A
ENST00000597442.5:n.133G>A
NM_000064.3:c.883G>A	NP_000055.2:p.Asp295Asn
NM_000064.4:c.883G>A MANE Select	NP_000055.2:p.Asp295Asn