Canonical Allele Identifier: CA505123235

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6684843G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684832G>T , CM000681.2:g.6684832G>T	GRCh38
NC_000019.9:g.6684843G>T , CM000681.1:g.6684843G>T	GRCh37
NC_000019.8:g.6635843G>T	NCBI36
NG_009557.1:g.40820C>A , LRG_27:g.40820C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2320C>A
ENST00000695653.1:c.1881C>A	ENSP00000512084.1:p.Thr627=
ENST00000695654.1:c.2997C>A	ENSP00000512085.1:p.Thr999=
ENST00000695690.1:n.163C>A
ENST00000695691.1:n.163C>A
ENST00000245907.11:c.3972C>A MANE Select	ENSP00000245907.4:p.Thr1324=
ENST00000245907.10:c.3972C>A	ENSP00000245907.4:p.Thr1324=
ENST00000596238.1:n.415C>A
ENST00000596548.1:c.54C>A	ENSP00000469744.1:p.Thr18=
ENST00000601008.1:c.241+1914C>A	ENSP00000471384.1:n.241+1914C>A
NM_000064.3:c.3972C>A	NP_000055.2:p.Thr1324=
NM_000064.4:c.3972C>A MANE Select	NP_000055.2:p.Thr1324=