Canonical Allele Identifier: CA348990365

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163124600A>T (hg19) ; chr2:g.162268090A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162268090A>T , CM000664.2:g.162268090A>T	GRCh38
NC_000002.11:g.163124600A>T , CM000664.1:g.163124600A>T	GRCh37
NC_000002.10:g.162832846A>T	NCBI36
NG_011495.1:g.55440T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*2401T>A	ENSP00000513228.1:n.*2401T>A
ENST00000648433.1:c.2687T>A	ENSP00000496816.1:p.Phe896Tyr
ENST00000649426.1:n.48T>A
ENST00000649554.1:n.2414T>A
ENST00000649979.2:c.2804T>A MANE Select	ENSP00000497271.1:p.Phe935Tyr
ENST00000679938.1:c.2492T>A	ENSP00000505518.1:p.Phe831Tyr
ENST00000263642.2:c.2804T>A	ENSP00000263642.2:p.Phe935Tyr
NM_022168.3:c.2804T>A	NP_071451.2:p.Phe935Tyr
XM_011511628.1:c.2087T>A	XP_011509930.1:p.Phe696Tyr
NM_022168.4:c.2804T>A MANE Select	NP_071451.2:p.Phe935Tyr