Canonical Allele Identifier: CA403632966

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697459A>T (hg19) ; chr19:g.6697448A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697448A>T , CM000681.2:g.6697448A>T	GRCh38
NC_000019.9:g.6697459A>T , CM000681.1:g.6697459A>T	GRCh37
NC_000019.8:g.6648459A>T	NCBI36
NG_009557.1:g.28204T>A , LRG_27:g.28204T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1040T>A
ENST00000695652.1:c.2569T>A	ENSP00000512083.1:p.Tyr857Asn
ENST00000695653.1:c.601T>A	ENSP00000512084.1:p.Tyr201Asn
ENST00000695654.1:c.1816T>A	ENSP00000512085.1:p.Tyr606Asn
ENST00000695655.1:c.1633T>A	ENSP00000512086.1:n.1633T>A
ENST00000695692.1:n.2056T>A
ENST00000245907.11:c.2692T>A MANE Select	ENSP00000245907.4:p.Tyr898Asn
ENST00000245907.10:c.2692T>A	ENSP00000245907.4:p.Tyr898Asn
ENST00000594005.1:n.268T>A
NM_000064.3:c.2692T>A	NP_000055.2:p.Tyr898Asn
NM_000064.4:c.2692T>A MANE Select	NP_000055.2:p.Tyr898Asn