Canonical Allele Identifier: CA403614794

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6681996T>A (hg19) ; chr19:g.6681985T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681985T>A , CM000681.2:g.6681985T>A	GRCh38
NC_000019.9:g.6681996T>A , CM000681.1:g.6681996T>A	GRCh37
NC_000019.8:g.6632996T>A	NCBI36
NG_009557.1:g.43667A>T , LRG_27:g.43667A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2654A>T
ENST00000695653.1:c.2215A>T	ENSP00000512084.1:p.Lys739Ter
ENST00000695654.1:c.3331A>T	ENSP00000512085.1:p.Lys1111Ter
ENST00000695689.1:c.277A>T	ENSP00000512101.1:n.277A>T
ENST00000695690.1:n.497A>T
ENST00000695691.1:n.497A>T
ENST00000245907.11:c.4306A>T MANE Select	ENSP00000245907.4:p.Lys1436Ter
ENST00000245907.10:c.4306A>T	ENSP00000245907.4:p.Lys1436Ter
ENST00000596548.1:c.427A>T	ENSP00000469744.1:p.Lys143Ter
ENST00000599899.5:n.1265A>T
ENST00000601008.1:c.242-4027A>T	ENSP00000471384.1:n.242-4027A>T
NM_000064.3:c.4306A>T	NP_000055.2:p.Lys1436Ter
NM_000064.4:c.4306A>T MANE Select	NP_000055.2:p.Lys1436Ter