Canonical Allele Identifier: CA403614538

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6681965A>T (hg19) ; chr19:g.6681954A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681954A>T , CM000681.2:g.6681954A>T	GRCh38
NC_000019.9:g.6681965A>T , CM000681.1:g.6681965A>T	GRCh37
NC_000019.8:g.6632965A>T	NCBI36
NG_009557.1:g.43698T>A , LRG_27:g.43698T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2685T>A
ENST00000695653.1:c.2246T>A	ENSP00000512084.1:p.Ile749Asn
ENST00000695654.1:c.3362T>A	ENSP00000512085.1:p.Ile1121Asn
ENST00000695689.1:c.308T>A	ENSP00000512101.1:n.308T>A
ENST00000695690.1:n.528T>A
ENST00000695691.1:n.528T>A
ENST00000245907.11:c.4337T>A MANE Select	ENSP00000245907.4:p.Ile1446Asn
ENST00000245907.10:c.4337T>A	ENSP00000245907.4:p.Ile1446Asn
ENST00000596548.1:c.458T>A	ENSP00000469744.1:p.Ile153Asn
ENST00000599899.5:n.1296T>A
ENST00000601008.1:c.242-3996T>A	ENSP00000471384.1:n.242-3996T>A
NM_000064.3:c.4337T>A	NP_000055.2:p.Ile1446Asn
NM_000064.4:c.4337T>A MANE Select	NP_000055.2:p.Ile1446Asn