Canonical Allele Identifier: CA403619593

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686190A>T (hg19) ; chr19:g.6686179A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686179A>T , CM000681.2:g.6686179A>T	GRCh38
NC_000019.9:g.6686190A>T , CM000681.1:g.6686190A>T	GRCh37
NC_000019.8:g.6637190A>T	NCBI36
NG_009557.1:g.39473T>A , LRG_27:g.39473T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2103T>A
ENST00000695652.1:c.3632T>A	ENSP00000512083.1:p.Val1211Asp
ENST00000695653.1:c.1664T>A	ENSP00000512084.1:p.Val555Asp
ENST00000695654.1:c.2780T>A	ENSP00000512085.1:p.Val927Asp
ENST00000695655.1:c.2696T>A	ENSP00000512086.1:n.2696T>A
ENST00000695692.1:n.3119T>A
ENST00000245907.11:c.3755T>A MANE Select	ENSP00000245907.4:p.Val1252Asp
ENST00000245907.10:c.3755T>A	ENSP00000245907.4:p.Val1252Asp
ENST00000596238.1:n.198T>A
ENST00000601008.1:c.241+567T>A	ENSP00000471384.1:n.241+567T>A
NM_000064.3:c.3755T>A	NP_000055.2:p.Val1252Asp
NM_000064.4:c.3755T>A MANE Select	NP_000055.2:p.Val1252Asp