Canonical Allele Identifier: CA505192444

Gene: C3

Linked Data

• dbSNP Id: rs1474972273
• MyVariant Identifiers: chr19:g.6697675G>A (hg19) ; chr19:g.6697664G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697664G>A , CM000681.2:g.6697664G>A	GRCh38
NC_000019.9:g.6697675G>A , CM000681.1:g.6697675G>A	GRCh37
NC_000019.8:g.6648675G>A	NCBI36
NG_009557.1:g.27988C>T , LRG_27:g.27988C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.919C>T
ENST00000695652.1:c.2448C>T	ENSP00000512083.1:p.Asn816=
ENST00000695653.1:c.480C>T	ENSP00000512084.1:p.Asn160=
ENST00000695654.1:c.1695C>T	ENSP00000512085.1:p.Asn565=
ENST00000695655.1:c.1512C>T	ENSP00000512086.1:n.1512C>T
ENST00000695692.1:n.1935C>T
ENST00000245907.11:c.2571C>T MANE Select	ENSP00000245907.4:p.Asn857=
ENST00000245907.10:c.2571C>T	ENSP00000245907.4:p.Asn857=
ENST00000594005.1:n.52C>T
ENST00000602053.1:n.619C>T
NM_000064.3:c.2571C>T	NP_000055.2:p.Asn857=
NM_000064.4:c.2571C>T MANE Select	NP_000055.2:p.Asn857=