Canonical Allele Identifier: CA59665801

Gene: IFIH1

Linked Data

• dbSNP Id: rs994007314
• MyVariant Identifiers: chr2:g.163138936T>C (hg19) ; chr2:g.162282426T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282426T>C , CM000664.2:g.162282426T>C	GRCh38
NC_000002.11:g.163138936T>C , CM000664.1:g.163138936T>C	GRCh37
NC_000002.10:g.162847182T>C	NCBI36
NG_011495.1:g.41104A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*843A>G	ENSP00000513228.1:n.*843A>G
ENST00000648433.1:c.1246A>G	ENSP00000496816.1:p.Ile416Val
ENST00000649554.1:n.856A>G
ENST00000649979.2:c.1246A>G MANE Select	ENSP00000497271.1:p.Ile416Val
ENST00000679938.1:c.934A>G	ENSP00000505518.1:p.Ile312Val
ENST00000263642.2:c.1246A>G	ENSP00000263642.2:p.Ile416Val
NM_022168.3:c.1246A>G	NP_071451.2:p.Ile416Val
XM_011511628.1:c.529A>G	XP_011509930.1:p.Ile177Val
XM_011511629.1:c.1246A>G	XP_011509931.1:p.Ile416Val
NM_022168.4:c.1246A>G MANE Select	NP_071451.2:p.Ile416Val