Canonical Allele Identifier: CA2754315657
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060501_219060508del , CM000664.2:g.219060501_219060508del GRCh38
NC_000002.11:g.219925223_219925230del , CM000664.1:g.219925223_219925230del GRCh37
NC_000002.10:g.219633467_219633474del NCBI36
NG_016741.1:g.5012_5019del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-38_-31del MANE Select ENSP00000295731.5:n.-38_-31del
NM_002181.3:c.-38_-31del NP_002172.2:n.-38_-31del
NM_002181.4:c.-38_-31del MANE Select NP_002172.2:n.-38_-31del