Canonical Allele Identifier: CA403632755

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697410G>T (hg19) ; chr19:g.6697399G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697399G>T , CM000681.2:g.6697399G>T	GRCh38
NC_000019.9:g.6697410G>T , CM000681.1:g.6697410G>T	GRCh37
NC_000019.8:g.6648410G>T	NCBI36
NG_009557.1:g.28253C>A , LRG_27:g.28253C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1089C>A
ENST00000695652.1:c.2618C>A	ENSP00000512083.1:p.Ala873Asp
ENST00000695653.1:c.650C>A	ENSP00000512084.1:p.Ala217Asp
ENST00000695654.1:c.1865C>A	ENSP00000512085.1:p.Ala622Asp
ENST00000695655.1:c.1682C>A	ENSP00000512086.1:n.1682C>A
ENST00000695692.1:n.2105C>A
ENST00000245907.11:c.2741C>A MANE Select	ENSP00000245907.4:p.Ala914Asp
ENST00000245907.10:c.2741C>A	ENSP00000245907.4:p.Ala914Asp
ENST00000594005.1:n.317C>A
NM_000064.3:c.2741C>A	NP_000055.2:p.Ala914Asp
NM_000064.4:c.2741C>A MANE Select	NP_000055.2:p.Ala914Asp