Canonical Allele Identifier: CA505120409

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679464T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679453T>A , CM000681.2:g.6679453T>A	GRCh38
NC_000019.9:g.6679464T>A , CM000681.1:g.6679464T>A	GRCh37
NC_000019.8:g.6630464T>A	NCBI36
NG_009557.1:g.46199A>T , LRG_27:g.46199A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2848A>T
ENST00000695653.1:c.2409A>T	ENSP00000512084.1:p.Gly803=
ENST00000695654.1:c.3525A>T	ENSP00000512085.1:p.Gly1175=
ENST00000695689.1:c.471A>T	ENSP00000512101.1:n.471A>T
ENST00000695690.1:n.1565A>T
ENST00000695691.1:n.1361A>T
ENST00000245907.11:c.4500A>T MANE Select	ENSP00000245907.4:p.Gly1500=
ENST00000245907.10:c.4500A>T	ENSP00000245907.4:p.Gly1500=
ENST00000599668.1:n.95A>T
ENST00000599899.5:n.1459A>T
ENST00000601008.1:c.242-1495A>T	ENSP00000471384.1:n.242-1495A>T
NM_000064.3:c.4500A>T	NP_000055.2:p.Gly1500=
NM_000064.4:c.4500A>T MANE Select	NP_000055.2:p.Gly1500=