Canonical Allele Identifier: CA1329042684
Gene: IHH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060401_219060404delinsGCAC , CM000664.2:g.219060401_219060404delinsGCAC GRCh38
NC_000002.11:g.219925123_219925126delinsGCAC , CM000664.1:g.219925123_219925126delinsGCAC GRCh37
NC_000002.10:g.219633367_219633370delinsGCAC NCBI36
NG_016741.1:g.5113_5116delinsGTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.64_67delinsGTGC MANE Select ENSP00000295731.5:p.Val22=
ENST00000295731.6:c.64_67delinsGTGC ENSP00000295731.5:p.Val22=
NM_002181.3:c.64_67delinsGTGC NP_002172.2:p.Val22=
NM_002181.4:c.64_67delinsGTGC MANE Select NP_002172.2:p.Val22=
Search 100 bp 5'
Search 100 bp 3'