Canonical Allele Identifier: CA349002466

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163137985C>G (hg19) ; chr2:g.162281475C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162281475C>G , CM000664.2:g.162281475C>G	GRCh38
NC_000002.11:g.163137985C>G , CM000664.1:g.163137985C>G	GRCh37
NC_000002.10:g.162846231C>G	NCBI36
NG_011495.1:g.42055G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697291.1:c.*974G>C	ENSP00000513228.1:n.*974G>C
ENST00000648433.1:c.1377G>C	ENSP00000496816.1:p.Arg459Ser
ENST00000649554.1:n.987G>C
ENST00000649979.2:c.1377G>C MANE Select	ENSP00000497271.1:p.Arg459Ser
ENST00000679938.1:c.1065G>C	ENSP00000505518.1:p.Arg355Ser
ENST00000263642.2:c.1377G>C	ENSP00000263642.2:p.Arg459Ser
NM_022168.3:c.1377G>C	NP_071451.2:p.Arg459Ser
XM_011511628.1:c.660G>C	XP_011509930.1:p.Arg220Ser
XM_011511629.1:c.1377G>C	XP_011509931.1:p.Arg459Ser
NM_022168.4:c.1377G>C MANE Select	NP_071451.2:p.Arg459Ser