Canonical Allele Identifier: CA1303149228
Gene: IFIH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162282261A= , CM000664.2:g.162282261A= GRCh38
NC_000002.11:g.163138771A= , CM000664.1:g.163138771A= GRCh37
NC_000002.10:g.162847017A= NCBI36
NG_011495.1:g.41269T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697291.1:c.*903+105T= ENSP00000513228.1:n.*903+105T=
ENST00000648433.1:c.1306+105T= ENSP00000496816.1:n.1306+105T=
ENST00000649554.1:n.916+105T=
ENST00000649979.2:c.1306+105T= MANE Select ENSP00000497271.1:n.1306+105T=
ENST00000679938.1:c.994+105T= ENSP00000505518.1:n.994+105T=
ENST00000263642.2:c.1306+105T= ENSP00000263642.2:n.1306+105T=
NM_022168.3:c.1306+105T= NP_071451.2:n.1306+105T=
XM_011511628.1:c.589+105T= XP_011509930.1:n.589+105T=
XM_011511629.1:c.1306+105T= XP_011509931.1:n.1306+105T=
NM_022168.4:c.1306+105T= MANE Select NP_071451.2:n.1306+105T=