Canonical Allele Identifier: CA1042494192
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs1948872941
gnomAD v3: 2-219060548-GC-G
gnomAD v4: 2-219060548-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060549del , CM000664.2:g.219060549del GRCh38
NC_000002.11:g.219925271del , CM000664.1:g.219925271del GRCh37
NC_000002.10:g.219633515del NCBI36
NG_016741.1:g.4968del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-82del MANE Select ENSP00000295731.5:n.-82del
NM_002181.4:c.-82del MANE Select NP_002172.2:n.-82del
Search 100 bp 5'
Search 100 bp 3'