Canonical Allele Identifier: CA348990391

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163124601A>T (hg19) ; chr2:g.162268091A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162268091A>T , CM000664.2:g.162268091A>T	GRCh38
NC_000002.11:g.163124601A>T , CM000664.1:g.163124601A>T	GRCh37
NC_000002.10:g.162832847A>T	NCBI36
NG_011495.1:g.55439T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*2400T>A	ENSP00000513228.1:n.*2400T>A
ENST00000648433.1:c.2686T>A	ENSP00000496816.1:p.Phe896Ile
ENST00000649426.1:n.47T>A
ENST00000649554.1:n.2413T>A
ENST00000649979.2:c.2803T>A MANE Select	ENSP00000497271.1:p.Phe935Ile
ENST00000679938.1:c.2491T>A	ENSP00000505518.1:p.Phe831Ile
ENST00000263642.2:c.2803T>A	ENSP00000263642.2:p.Phe935Ile
NM_022168.3:c.2803T>A	NP_071451.2:p.Phe935Ile
XM_011511628.1:c.2086T>A	XP_011509930.1:p.Phe696Ile
NM_022168.4:c.2803T>A MANE Select	NP_071451.2:p.Phe935Ile