Canonical Allele Identifier: CA348990039

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163124062C>G (hg19) ; chr2:g.162267552C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162267552C>G , CM000664.2:g.162267552C>G	GRCh38
NC_000002.11:g.163124062C>G , CM000664.1:g.163124062C>G	GRCh37
NC_000002.10:g.162832308C>G	NCBI36
NG_011495.1:g.55978G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697291.1:c.*2422G>C	ENSP00000513228.1:n.*2422G>C
ENST00000648433.1:c.2708G>C	ENSP00000496816.1:p.Arg903Thr
ENST00000649426.1:n.586G>C
ENST00000649554.1:n.2435G>C
ENST00000649979.2:c.2825G>C MANE Select	ENSP00000497271.1:p.Arg942Thr
ENST00000679938.1:c.2513G>C	ENSP00000505518.1:p.Arg838Thr
ENST00000263642.2:c.2825G>C	ENSP00000263642.2:p.Arg942Thr
NM_022168.3:c.2825G>C	NP_071451.2:p.Arg942Thr
XM_011511628.1:c.2108G>C	XP_011509930.1:p.Arg703Thr
NM_022168.4:c.2825G>C MANE Select	NP_071451.2:p.Arg942Thr