Canonical Allele Identifier: CA1303149280
Gene: IFIH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162282349T= , CM000664.2:g.162282349T= GRCh38
NC_000002.11:g.163138859T= , CM000664.1:g.163138859T= GRCh37
NC_000002.10:g.162847105T= NCBI36
NG_011495.1:g.41181A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697291.1:c.*903+17A= ENSP00000513228.1:n.*903+17A=
ENST00000648433.1:c.1306+17A= ENSP00000496816.1:n.1306+17A=
ENST00000649554.1:n.916+17A=
ENST00000649979.2:c.1306+17A= MANE Select ENSP00000497271.1:n.1306+17A=
ENST00000679938.1:c.994+17A= ENSP00000505518.1:n.994+17A=
ENST00000263642.2:c.1306+17A= ENSP00000263642.2:n.1306+17A=
NM_022168.3:c.1306+17A= NP_071451.2:n.1306+17A=
XM_011511628.1:c.589+17A= XP_011509930.1:n.589+17A=
XM_011511629.1:c.1306+17A= XP_011509931.1:n.1306+17A=
NM_022168.4:c.1306+17A= MANE Select NP_071451.2:n.1306+17A=