Canonical Allele Identifier: CA403614420

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6681956T>A (hg19) ; chr19:g.6681945T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681945T>A , CM000681.2:g.6681945T>A	GRCh38
NC_000019.9:g.6681956T>A , CM000681.1:g.6681956T>A	GRCh37
NC_000019.8:g.6632956T>A	NCBI36
NG_009557.1:g.43707A>T , LRG_27:g.43707A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2694A>T
ENST00000695653.1:c.2255A>T	ENSP00000512084.1:p.Asp752Val
ENST00000695654.1:c.3371A>T	ENSP00000512085.1:p.Asp1124Val
ENST00000695689.1:c.317A>T	ENSP00000512101.1:n.317A>T
ENST00000695690.1:n.537A>T
ENST00000695691.1:n.537A>T
ENST00000245907.11:c.4346A>T MANE Select	ENSP00000245907.4:p.Asp1449Val
ENST00000245907.10:c.4346A>T	ENSP00000245907.4:p.Asp1449Val
ENST00000596548.1:c.467A>T	ENSP00000469744.1:p.Asp156Val
ENST00000599899.5:n.1305A>T
ENST00000601008.1:c.242-3987A>T	ENSP00000471384.1:n.242-3987A>T
NM_000064.3:c.4346A>T	NP_000055.2:p.Asp1449Val
NM_000064.4:c.4346A>T MANE Select	NP_000055.2:p.Asp1449Val