Canonical Allele Identifier: CA1303141158
Gene: IFIH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162267441T= , CM000664.2:g.162267441T= GRCh38
NC_000002.11:g.163123951T= , CM000664.1:g.163123951T= GRCh37
NC_000002.10:g.162832197T= NCBI36
NG_011495.1:g.56089A=

Transcript Alleles

HGVS Amino-acid change
ENST00000697291.1:c.*2495+38A= ENSP00000513228.1:n.*2495+38A=
ENST00000648433.1:c.2781+38A= ENSP00000496816.1:n.2781+38A=
ENST00000649426.1:n.659+38A=
ENST00000649554.1:n.2508+38A=
ENST00000649979.2:c.2898+38A= MANE Select ENSP00000497271.1:n.2898+38A=
ENST00000679938.1:c.2586+38A= ENSP00000505518.1:n.2586+38A=
ENST00000263642.2:c.2898+38A= ENSP00000263642.2:n.2898+38A=
NM_022168.3:c.2898+38A= NP_071451.2:n.2898+38A=
XM_011511628.1:c.2181+38A= XP_011509930.1:n.2181+38A=
NM_022168.4:c.2898+38A= MANE Select NP_071451.2:n.2898+38A=