Canonical Allele Identifier: CA348990474

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163124609G>A (hg19) ; chr2:g.162268099G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162268099G>A , CM000664.2:g.162268099G>A	GRCh38
NC_000002.11:g.163124609G>A , CM000664.1:g.163124609G>A	GRCh37
NC_000002.10:g.162832855G>A	NCBI36
NG_011495.1:g.55431C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697291.1:c.*2392C>T	ENSP00000513228.1:n.*2392C>T
ENST00000648433.1:c.2678C>T	ENSP00000496816.1:p.Thr893Ile
ENST00000649426.1:n.39C>T
ENST00000649554.1:n.2405C>T
ENST00000649979.2:c.2795C>T MANE Select	ENSP00000497271.1:p.Thr932Ile
ENST00000679938.1:c.2483C>T	ENSP00000505518.1:p.Thr828Ile
ENST00000263642.2:c.2795C>T	ENSP00000263642.2:p.Thr932Ile
NM_022168.3:c.2795C>T	NP_071451.2:p.Thr932Ile
XM_011511628.1:c.2078C>T	XP_011509930.1:p.Thr693Ile
NM_022168.4:c.2795C>T MANE Select	NP_071451.2:p.Thr932Ile