Canonical Allele Identifier: CA505193177

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713499C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713488C>A , CM000681.2:g.6713488C>A	GRCh38
NC_000019.9:g.6713499C>A , CM000681.1:g.6713499C>A	GRCh37
NC_000019.8:g.6664499C>A	NCBI36
NG_009557.1:g.12164G>T , LRG_27:g.12164G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.672G>T	ENSP00000512083.1:p.Val224=
ENST00000695692.1:n.119G>T
ENST00000245907.11:c.795G>T MANE Select	ENSP00000245907.4:p.Val265=
ENST00000245907.10:c.795G>T	ENSP00000245907.4:p.Val265=
ENST00000595577.1:n.299G>T
ENST00000597442.5:n.45G>T
NM_000064.3:c.795G>T	NP_000055.2:p.Val265=
NM_000064.4:c.795G>T MANE Select	NP_000055.2:p.Val265=