Canonical Allele Identifier: CA505192516

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697732A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697721A>T , CM000681.2:g.6697721A>T	GRCh38
NC_000019.9:g.6697732A>T , CM000681.1:g.6697732A>T	GRCh37
NC_000019.8:g.6648732A>T	NCBI36
NG_009557.1:g.27931T>A , LRG_27:g.27931T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.862T>A
ENST00000695652.1:c.2391T>A	ENSP00000512083.1:p.Ser797=
ENST00000695653.1:c.423T>A	ENSP00000512084.1:p.Ser141=
ENST00000695654.1:c.1638T>A	ENSP00000512085.1:p.Ser546=
ENST00000695655.1:c.1455T>A	ENSP00000512086.1:n.1455T>A
ENST00000695692.1:n.1878T>A
ENST00000245907.11:c.2514T>A MANE Select	ENSP00000245907.4:p.Ser838=
ENST00000245907.10:c.2514T>A	ENSP00000245907.4:p.Ser838=
ENST00000602053.1:n.562T>A
NM_000064.3:c.2514T>A	NP_000055.2:p.Ser838=
NM_000064.4:c.2514T>A MANE Select	NP_000055.2:p.Ser838=