Canonical Allele Identifier: CA2663195374
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060543-CGGGGGCTCAGGCGTCCGGGTGGCTCCG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060552_219060578del , CM000664.2:g.219060552_219060578del GRCh38
NC_000002.11:g.219925274_219925300del , CM000664.1:g.219925274_219925300del GRCh37
NC_000002.10:g.219633518_219633544del NCBI36
NG_016741.1:g.4947_4973del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-103_-77del MANE Select ENSP00000295731.5:n.-103_-77del
NM_002181.4:c.-103_-77del MANE Select NP_002172.2:n.-103_-77del
Search 100 bp 5'
Search 100 bp 3'