Canonical Allele Identifier: CA505122339

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6682024G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682013G>A , CM000681.2:g.6682013G>A	GRCh38
NC_000019.9:g.6682024G>A , CM000681.1:g.6682024G>A	GRCh37
NC_000019.8:g.6633024G>A	NCBI36
NG_009557.1:g.43639C>T , LRG_27:g.43639C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2626C>T
ENST00000695653.1:c.2187C>T	ENSP00000512084.1:p.Asp729=
ENST00000695654.1:c.3303C>T	ENSP00000512085.1:p.Asp1101=
ENST00000695689.1:c.249C>T	ENSP00000512101.1:n.249C>T
ENST00000695690.1:n.469C>T
ENST00000695691.1:n.469C>T
ENST00000245907.11:c.4278C>T MANE Select	ENSP00000245907.4:p.Asp1426=
ENST00000245907.10:c.4278C>T	ENSP00000245907.4:p.Asp1426=
ENST00000596548.1:c.399C>T	ENSP00000469744.1:p.Asp133=
ENST00000599899.5:n.1237C>T
ENST00000601008.1:c.242-4055C>T	ENSP00000471384.1:n.242-4055C>T
NM_000064.3:c.4278C>T	NP_000055.2:p.Asp1426=
NM_000064.4:c.4278C>T MANE Select	NP_000055.2:p.Asp1426=