Canonical Allele Identifier: CA2577248549
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060082-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060087del , CM000664.2:g.219060087del GRCh38
NC_000002.11:g.219924809del , CM000664.1:g.219924809del GRCh37
NC_000002.10:g.219633053del NCBI36
NG_016741.1:g.5434del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.315+70del MANE Select ENSP00000295731.5:n.315+70del
ENST00000295731.6:c.315+70del ENSP00000295731.5:n.315+70del
NM_002181.3:c.315+70del NP_002172.2:n.315+70del
NM_002181.4:c.315+70del MANE Select NP_002172.2:n.315+70del
Search 100 bp 5'
Search 100 bp 3'