Canonical Allele Identifier: CA348990370

Gene: IFIH1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*2400T>G	ENSP00000513228.1:n.*2400T>G
ENST00000648433.1:c.2686T>G	ENSP00000496816.1:p.Phe896Val
ENST00000649426.1:n.47T>G
ENST00000649554.1:n.2413T>G
ENST00000649979.2:c.2803T>G MANE Select	ENSP00000497271.1:p.Phe935Val
ENST00000679938.1:c.2491T>G	ENSP00000505518.1:p.Phe831Val
ENST00000263642.2:c.2803T>G	ENSP00000263642.2:p.Phe935Val
NM_022168.3:c.2803T>G	NP_071451.2:p.Phe935Val
XM_011511628.1:c.2086T>G	XP_011509930.1:p.Phe696Val
NM_022168.4:c.2803T>G MANE Select	NP_071451.2:p.Phe935Val