Canonical Allele Identifier: CA2663195331
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060508-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060511del , CM000664.2:g.219060511del GRCh38
NC_000002.11:g.219925233del , CM000664.1:g.219925233del GRCh37
NC_000002.10:g.219633477del NCBI36
NG_016741.1:g.5008del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-42del MANE Select ENSP00000295731.5:n.-42del
NM_002181.3:c.-42del NP_002172.2:n.-42del
NM_002181.4:c.-42del MANE Select NP_002172.2:n.-42del
Search 100 bp 5'
Search 100 bp 3'