Canonical Allele Identifier: CA2663194959
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060087-GT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060088del , CM000664.2:g.219060088del GRCh38
NC_000002.11:g.219924810del , CM000664.1:g.219924810del GRCh37
NC_000002.10:g.219633054del NCBI36
NG_016741.1:g.5429del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.315+65del MANE Select ENSP00000295731.5:n.315+65del
ENST00000295731.6:c.315+65del ENSP00000295731.5:n.315+65del
NM_002181.3:c.315+65del NP_002172.2:n.315+65del
NM_002181.4:c.315+65del MANE Select NP_002172.2:n.315+65del
Search 100 bp 5'
Search 100 bp 3'