Canonical Allele Identifier: CA2663195165
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060416-GCAA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060419_219060421del , CM000664.2:g.219060419_219060421del GRCh38
NC_000002.11:g.219925141_219925143del , CM000664.1:g.219925141_219925143del GRCh37
NC_000002.10:g.219633385_219633387del NCBI36
NG_016741.1:g.5098_5100del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.49_51del MANE Select ENSP00000295731.5:p.Leu17del
ENST00000295731.6:c.49_51del ENSP00000295731.5:p.Leu17del
NM_002181.3:c.49_51del NP_002172.2:p.Leu17del
NM_002181.4:c.49_51del MANE Select NP_002172.2:p.Leu17del
Search 100 bp 5'
Search 100 bp 3'