Canonical Allele Identifier: CA349002911

Gene: IFIH1

Linked Data

• MyVariant Identifiers: chr2:g.163139002T>C (hg19) ; chr2:g.162282492T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282492T>C , CM000664.2:g.162282492T>C	GRCh38
NC_000002.11:g.163139002T>C , CM000664.1:g.163139002T>C	GRCh37
NC_000002.10:g.162847248T>C	NCBI36
NG_011495.1:g.41038A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*777A>G	ENSP00000513228.1:n.*777A>G
ENST00000648433.1:c.1180A>G	ENSP00000496816.1:p.Thr394Ala
ENST00000649554.1:n.790A>G
ENST00000649979.2:c.1180A>G MANE Select	ENSP00000497271.1:p.Thr394Ala
ENST00000679938.1:c.868A>G	ENSP00000505518.1:p.Thr290Ala
ENST00000263642.2:c.1180A>G	ENSP00000263642.2:p.Thr394Ala
NM_022168.3:c.1180A>G	NP_071451.2:p.Thr394Ala
XM_011511628.1:c.463A>G	XP_011509930.1:p.Thr155Ala
XM_011511629.1:c.1180A>G	XP_011509931.1:p.Thr394Ala
NM_022168.4:c.1180A>G MANE Select	NP_071451.2:p.Thr394Ala