Canonical Allele Identifier: CA403612758

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679457T>A (hg19) ; chr19:g.6679446T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679446T>A , CM000681.2:g.6679446T>A	GRCh38
NC_000019.9:g.6679457T>A , CM000681.1:g.6679457T>A	GRCh37
NC_000019.8:g.6630457T>A	NCBI36
NG_009557.1:g.46206A>T , LRG_27:g.46206A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2855A>T
ENST00000695653.1:c.2416A>T	ENSP00000512084.1:p.Asn806Tyr
ENST00000695654.1:c.3532A>T	ENSP00000512085.1:p.Asn1178Tyr
ENST00000695689.1:c.478A>T	ENSP00000512101.1:n.478A>T
ENST00000695690.1:n.1572A>T
ENST00000695691.1:n.1368A>T
ENST00000245907.11:c.4507A>T MANE Select	ENSP00000245907.4:p.Asn1503Tyr
ENST00000245907.10:c.4507A>T	ENSP00000245907.4:p.Asn1503Tyr
ENST00000599668.1:n.102A>T
ENST00000599899.5:n.1466A>T
ENST00000601008.1:c.242-1488A>T	ENSP00000471384.1:n.242-1488A>T
NM_000064.3:c.4507A>T	NP_000055.2:p.Asn1503Tyr
NM_000064.4:c.4507A>T MANE Select	NP_000055.2:p.Asn1503Tyr