Canonical Allele Identifier: CA403642340

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713316C>T (hg19) ; chr19:g.6713305C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713305C>T , CM000681.2:g.6713305C>T	GRCh38
NC_000019.9:g.6713316C>T , CM000681.1:g.6713316C>T	GRCh37
NC_000019.8:g.6664316C>T	NCBI36
NG_009557.1:g.12347G>A , LRG_27:g.12347G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.764G>A	ENSP00000512083.1:p.Gly255Asp
ENST00000695654.1:c.11G>A	ENSP00000512085.1:p.Gly4Asp
ENST00000695692.1:n.211G>A
ENST00000245907.11:c.887G>A MANE Select	ENSP00000245907.4:p.Gly296Asp
ENST00000245907.10:c.887G>A	ENSP00000245907.4:p.Gly296Asp
ENST00000594270.5:n.11G>A
ENST00000595577.1:n.391G>A
ENST00000597442.5:n.137G>A
NM_000064.3:c.887G>A	NP_000055.2:p.Gly296Asp
NM_000064.4:c.887G>A MANE Select	NP_000055.2:p.Gly296Asp