Canonical Allele Identifier: CA2577248584
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060563-TGGCTCCGGGG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060570_219060579del , CM000664.2:g.219060570_219060579del GRCh38
NC_000002.11:g.219925292_219925301del , CM000664.1:g.219925292_219925301del GRCh37
NC_000002.10:g.219633536_219633545del NCBI36
NG_016741.1:g.4944_4953del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-106_-97del MANE Select ENSP00000295731.5:n.-106_-97del
NM_002181.4:c.-106_-97del MANE Select NP_002172.2:n.-106_-97del
Search 100 bp 5'
Search 100 bp 3'