Canonical Allele Identifier: CA349002789
Gene: IFIH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162282435T>C , CM000664.2:g.162282435T>C GRCh38
NC_000002.11:g.163138945T>C , CM000664.1:g.163138945T>C GRCh37
NC_000002.10:g.162847191T>C NCBI36
NG_011495.1:g.41095A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697291.1:c.*834A>G ENSP00000513228.1:n.*834A>G
ENST00000648433.1:c.1237A>G ENSP00000496816.1:p.Thr413Ala
ENST00000649554.1:n.847A>G
ENST00000649979.2:c.1237A>G MANE Select ENSP00000497271.1:p.Thr413Ala
ENST00000679938.1:c.925A>G ENSP00000505518.1:p.Thr309Ala
ENST00000263642.2:c.1237A>G ENSP00000263642.2:p.Thr413Ala
NM_022168.3:c.1237A>G NP_071451.2:p.Thr413Ala
XM_011511628.1:c.520A>G XP_011509930.1:p.Thr174Ala
XM_011511629.1:c.1237A>G XP_011509931.1:p.Thr413Ala
NM_022168.4:c.1237A>G MANE Select NP_071451.2:p.Thr413Ala