Canonical Allele Identifier: CA403618464

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685096T>A (hg19) ; chr19:g.6685085T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685085T>A , CM000681.2:g.6685085T>A	GRCh38
NC_000019.9:g.6685096T>A , CM000681.1:g.6685096T>A	GRCh37
NC_000019.8:g.6636096T>A	NCBI36
NG_009557.1:g.40567A>T , LRG_27:g.40567A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2220A>T
ENST00000695653.1:c.1781A>T	ENSP00000512084.1:p.Glu594Val
ENST00000695654.1:c.2897A>T	ENSP00000512085.1:p.Glu966Val
ENST00000695690.1:n.63A>T
ENST00000695691.1:n.63A>T
ENST00000245907.11:c.3872A>T MANE Select	ENSP00000245907.4:p.Glu1291Val
ENST00000245907.10:c.3872A>T	ENSP00000245907.4:p.Glu1291Val
ENST00000596238.1:n.315A>T
ENST00000601008.1:c.241+1661A>T	ENSP00000471384.1:n.241+1661A>T
NM_000064.3:c.3872A>T	NP_000055.2:p.Glu1291Val
NM_000064.4:c.3872A>T MANE Select	NP_000055.2:p.Glu1291Val