Canonical Allele Identifier: CA2661689019
Gene: IFIH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162281626T>G , CM000664.2:g.162281626T>G GRCh38
NC_000002.11:g.163138136T>G , CM000664.1:g.163138136T>G GRCh37
NC_000002.10:g.162846382T>G NCBI36
NG_011495.1:g.41904A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697291.1:c.*904-81A>C ENSP00000513228.1:n.*904-81A>C
ENST00000648433.1:c.1307-81A>C ENSP00000496816.1:n.1307-81A>C
ENST00000649554.1:n.917-81A>C
ENST00000649979.2:c.1307-81A>C MANE Select ENSP00000497271.1:n.1307-81A>C
ENST00000679938.1:c.995-81A>C ENSP00000505518.1:n.995-81A>C
ENST00000263642.2:c.1307-81A>C ENSP00000263642.2:n.1307-81A>C
NM_022168.3:c.1307-81A>C NP_071451.2:n.1307-81A>C
XM_011511628.1:c.590-81A>C XP_011509930.1:n.590-81A>C
XM_011511629.1:c.1307-81A>C XP_011509931.1:n.1307-81A>C
NM_022168.4:c.1307-81A>C MANE Select NP_071451.2:n.1307-81A>C