Canonical Allele Identifier: CA505193127

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713466C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713455C>T , CM000681.2:g.6713455C>T	GRCh38
NC_000019.9:g.6713466C>T , CM000681.1:g.6713466C>T	GRCh37
NC_000019.8:g.6664466C>T	NCBI36
NG_009557.1:g.12197G>A , LRG_27:g.12197G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.705G>A	ENSP00000512083.1:p.Gln235=
ENST00000695692.1:n.152G>A
ENST00000245907.11:c.828G>A MANE Select	ENSP00000245907.4:p.Gln276=
ENST00000245907.10:c.828G>A	ENSP00000245907.4:p.Gln276=
ENST00000595577.1:n.332G>A
ENST00000597442.5:n.78G>A
NM_000064.3:c.828G>A	NP_000055.2:p.Gln276=
NM_000064.4:c.828G>A MANE Select	NP_000055.2:p.Gln276=