Canonical Allele Identifier: CA403614878

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6682008A>T (hg19) ; chr19:g.6681997A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681997A>T , CM000681.2:g.6681997A>T	GRCh38
NC_000019.9:g.6682008A>T , CM000681.1:g.6682008A>T	GRCh37
NC_000019.8:g.6633008A>T	NCBI36
NG_009557.1:g.43655T>A , LRG_27:g.43655T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2642T>A
ENST00000695653.1:c.2203T>A	ENSP00000512084.1:p.Tyr735Asn
ENST00000695654.1:c.3319T>A	ENSP00000512085.1:p.Tyr1107Asn
ENST00000695689.1:c.265T>A	ENSP00000512101.1:n.265T>A
ENST00000695690.1:n.485T>A
ENST00000695691.1:n.485T>A
ENST00000245907.11:c.4294T>A MANE Select	ENSP00000245907.4:p.Tyr1432Asn
ENST00000245907.10:c.4294T>A	ENSP00000245907.4:p.Tyr1432Asn
ENST00000596548.1:c.415T>A	ENSP00000469744.1:p.Tyr139Asn
ENST00000599899.5:n.1253T>A
ENST00000601008.1:c.242-4039T>A	ENSP00000471384.1:n.242-4039T>A
NM_000064.3:c.4294T>A	NP_000055.2:p.Tyr1432Asn
NM_000064.4:c.4294T>A MANE Select	NP_000055.2:p.Tyr1432Asn