Canonical Allele Identifier: CA2520020050
Gene: IHH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060586_219060597del , CM000664.2:g.219060586_219060597del GRCh38
NC_000002.11:g.219925308_219925319del , CM000664.1:g.219925308_219925319del GRCh37
NC_000002.10:g.219633552_219633563del NCBI36
NG_016741.1:g.4922_4933del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-128_-117del MANE Select ENSP00000295731.5:n.-128_-117del
NM_002181.4:c.-128_-117del MANE Select NP_002172.2:n.-128_-117del
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