Canonical Allele Identifier: CA2663195157
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060407-CCAG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060416_219060418del , CM000664.2:g.219060416_219060418del GRCh38
NC_000002.11:g.219925138_219925140del , CM000664.1:g.219925138_219925140del GRCh37
NC_000002.10:g.219633382_219633384del NCBI36
NG_016741.1:g.5107_5109del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.58_60del MANE Select ENSP00000295731.5:p.Leu20del
ENST00000295731.6:c.58_60del ENSP00000295731.5:p.Leu20del
NM_002181.3:c.58_60del NP_002172.2:p.Leu20del
NM_002181.4:c.58_60del MANE Select NP_002172.2:p.Leu20del
Search 100 bp 5'
Search 100 bp 3'