Canonical Allele Identifier: CA429535979

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163138918A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282408A>G , CM000664.2:g.162282408A>G	GRCh38
NC_000002.11:g.163138918A>G , CM000664.1:g.163138918A>G	GRCh37
NC_000002.10:g.162847164A>G	NCBI36
NG_011495.1:g.41122T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697291.1:c.*861T>C	ENSP00000513228.1:n.*861T>C
ENST00000648433.1:c.1264T>C	ENSP00000496816.1:p.Leu422=
ENST00000649554.1:n.874T>C
ENST00000649979.2:c.1264T>C MANE Select	ENSP00000497271.1:p.Leu422=
ENST00000679938.1:c.952T>C	ENSP00000505518.1:p.Leu318=
ENST00000263642.2:c.1264T>C	ENSP00000263642.2:p.Leu422=
NM_022168.3:c.1264T>C	NP_071451.2:p.Leu422=
XM_011511628.1:c.547T>C	XP_011509930.1:p.Leu183=
XM_011511629.1:c.1264T>C	XP_011509931.1:p.Leu422=
NM_022168.4:c.1264T>C MANE Select	NP_071451.2:p.Leu422=