Canonical Allele Identifier: CA1038596357
Gene: IFIH1 HGNC NCBI

Linked Data

dbSNP Id: rs1682831691

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162282601A>G , CM000664.2:g.162282601A>G GRCh38
NC_000002.11:g.163139111A>G , CM000664.1:g.163139111A>G GRCh37
NC_000002.10:g.162847357A>G NCBI36
NG_011495.1:g.40929T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697291.1:c.*693-25T>C ENSP00000513228.1:n.*693-25T>C
ENST00000648433.1:c.1096-25T>C ENSP00000496816.1:n.1096-25T>C
ENST00000649554.1:n.706-25T>C
ENST00000649979.2:c.1096-25T>C MANE Select ENSP00000497271.1:n.1096-25T>C
ENST00000679938.1:c.784-25T>C ENSP00000505518.1:n.784-25T>C
ENST00000263642.2:c.1096-25T>C ENSP00000263642.2:n.1096-25T>C
NM_022168.3:c.1096-25T>C NP_071451.2:n.1096-25T>C
XM_011511628.1:c.379-25T>C XP_011509930.1:n.379-25T>C
XM_011511629.1:c.1096-25T>C XP_011509931.1:n.1096-25T>C
NM_022168.4:c.1096-25T>C MANE Select NP_071451.2:n.1096-25T>C