Canonical Allele Identifier: CA403645086

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6718290G>A (hg19) ; chr19:g.6718279G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6718279G>A , CM000681.2:g.6718279G>A	GRCh38
NC_000019.9:g.6718290G>A , CM000681.1:g.6718290G>A	GRCh37
NC_000019.8:g.6669290G>A	NCBI36
NG_009557.1:g.7373C>T , LRG_27:g.7373C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594936.2:n.462C>T
ENST00000695652.1:c.278C>T	ENSP00000512083.1:p.Thr93Ile
ENST00000695693.1:c.401C>T	ENSP00000512104.1:p.Thr134Ile
ENST00000245907.11:c.401C>T MANE Select	ENSP00000245907.4:p.Thr134Ile
ENST00000245907.10:c.401C>T	ENSP00000245907.4:p.Thr134Ile
ENST00000594936.1:n.462C>T
ENST00000600744.1:c.278C>T	ENSP00000472044.1:p.Thr93Ile
NM_000064.3:c.401C>T	NP_000055.2:p.Thr134Ile
NM_000064.4:c.401C>T MANE Select	NP_000055.2:p.Thr134Ile