Canonical Allele Identifier: CA2663195237
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060462-AGAC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060463_219060465del , CM000664.2:g.219060463_219060465del GRCh38
NC_000002.11:g.219925185_219925187del , CM000664.1:g.219925185_219925187del GRCh37
NC_000002.10:g.219633429_219633431del NCBI36
NG_016741.1:g.5052_5054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.3_5del MANE Select ENSP00000295731.5:p.Met1_Ser2delinsIle
ENST00000295731.6:c.3_5del ENSP00000295731.5:p.Met1_Ser2delinsIle
NM_002181.3:c.3_5del NP_002172.2:p.Met1_Ser2delinsIle
NM_002181.4:c.3_5del MANE Select NP_002172.2:p.Met1_Ser2delinsIle
Search 100 bp 5'
Search 100 bp 3'