Canonical Allele Identifier: CA403619385

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686149A>T (hg19) ; chr19:g.6686138A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686138A>T , CM000681.2:g.6686138A>T	GRCh38
NC_000019.9:g.6686149A>T , CM000681.1:g.6686149A>T	GRCh37
NC_000019.8:g.6637149A>T	NCBI36
NG_009557.1:g.39514T>A , LRG_27:g.39514T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2144T>A
ENST00000695652.1:c.3673T>A	ENSP00000512083.1:p.Tyr1225Asn
ENST00000695653.1:c.1705T>A	ENSP00000512084.1:p.Tyr569Asn
ENST00000695654.1:c.2821T>A	ENSP00000512085.1:p.Tyr941Asn
ENST00000695655.1:c.2737T>A	ENSP00000512086.1:n.2737T>A
ENST00000695692.1:n.3160T>A
ENST00000245907.11:c.3796T>A MANE Select	ENSP00000245907.4:p.Tyr1266Asn
ENST00000245907.10:c.3796T>A	ENSP00000245907.4:p.Tyr1266Asn
ENST00000596238.1:n.239T>A
ENST00000601008.1:c.241+608T>A	ENSP00000471384.1:n.241+608T>A
NM_000064.3:c.3796T>A	NP_000055.2:p.Tyr1266Asn
NM_000064.4:c.3796T>A MANE Select	NP_000055.2:p.Tyr1266Asn