Canonical Allele Identifier: CA2663195420
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060570-GGGGGGCTCCAGGC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060577_219060589del , CM000664.2:g.219060577_219060589del GRCh38
NC_000002.11:g.219925299_219925311del , CM000664.1:g.219925299_219925311del GRCh37
NC_000002.10:g.219633543_219633555del NCBI36
NG_016741.1:g.4934_4946del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-116_-104del MANE Select ENSP00000295731.5:n.-116_-104del
NM_002181.4:c.-116_-104del MANE Select NP_002172.2:n.-116_-104del
Search 100 bp 5'
Search 100 bp 3'