Canonical Allele Identifier: CA403619429

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686158C>A (hg19) ; chr19:g.6686147C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686147C>A , CM000681.2:g.6686147C>A	GRCh38
NC_000019.9:g.6686158C>A , CM000681.1:g.6686158C>A	GRCh37
NC_000019.8:g.6637158C>A	NCBI36
NG_009557.1:g.39505G>T , LRG_27:g.39505G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2135G>T
ENST00000695652.1:c.3664G>T	ENSP00000512083.1:p.Gly1222Cys
ENST00000695653.1:c.1696G>T	ENSP00000512084.1:p.Gly566Cys
ENST00000695654.1:c.2812G>T	ENSP00000512085.1:p.Gly938Cys
ENST00000695655.1:c.2728G>T	ENSP00000512086.1:n.2728G>T
ENST00000695692.1:n.3151G>T
ENST00000245907.11:c.3787G>T MANE Select	ENSP00000245907.4:p.Gly1263Cys
ENST00000245907.10:c.3787G>T	ENSP00000245907.4:p.Gly1263Cys
ENST00000596238.1:n.230G>T
ENST00000601008.1:c.241+599G>T	ENSP00000471384.1:n.241+599G>T
NM_000064.3:c.3787G>T	NP_000055.2:p.Gly1263Cys
NM_000064.4:c.3787G>T MANE Select	NP_000055.2:p.Gly1263Cys