Canonical Allele Identifier: CA403639351

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709762A>T (hg19) ; chr19:g.6709751A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709751A>T , CM000681.2:g.6709751A>T	GRCh38
NC_000019.9:g.6709762A>T , CM000681.1:g.6709762A>T	GRCh37
NC_000019.8:g.6660762A>T	NCBI36
NG_009557.1:g.15901T>A , LRG_27:g.15901T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1655T>A	ENSP00000512083.1:p.Val552Glu
ENST00000695654.1:c.902T>A	ENSP00000512085.1:p.Val301Glu
ENST00000695655.1:c.719T>A	ENSP00000512086.1:n.719T>A
ENST00000695692.1:n.1142T>A
ENST00000245907.11:c.1778T>A MANE Select	ENSP00000245907.4:p.Val593Glu
ENST00000245907.10:c.1778T>A	ENSP00000245907.4:p.Val593Glu
NM_000064.3:c.1778T>A	NP_000055.2:p.Val593Glu
NM_000064.4:c.1778T>A MANE Select	NP_000055.2:p.Val593Glu