Canonical Allele Identifier: CA403619850

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686236G>T (hg19) ; chr19:g.6686225G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686225G>T , CM000681.2:g.6686225G>T	GRCh38
NC_000019.9:g.6686236G>T , CM000681.1:g.6686236G>T	GRCh37
NC_000019.8:g.6637236G>T	NCBI36
NG_009557.1:g.39427C>A , LRG_27:g.39427C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2057C>A
ENST00000695652.1:c.3586C>A	ENSP00000512083.1:p.Leu1196Ile
ENST00000695653.1:c.1618C>A	ENSP00000512084.1:p.Leu540Ile
ENST00000695654.1:c.2734C>A	ENSP00000512085.1:p.Leu912Ile
ENST00000695655.1:c.2650C>A	ENSP00000512086.1:n.2650C>A
ENST00000695692.1:n.3073C>A
ENST00000245907.11:c.3709C>A MANE Select	ENSP00000245907.4:p.Leu1237Ile
ENST00000245907.10:c.3709C>A	ENSP00000245907.4:p.Leu1237Ile
ENST00000596238.1:n.152C>A
ENST00000601008.1:c.241+521C>A	ENSP00000471384.1:n.241+521C>A
NM_000064.3:c.3709C>A	NP_000055.2:p.Leu1237Ile
NM_000064.4:c.3709C>A MANE Select	NP_000055.2:p.Leu1237Ile