Canonical Allele Identifier: CA1329042590
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060198G= , CM000664.2:g.219060198G= GRCh38
NC_000002.11:g.219924920G= , CM000664.1:g.219924920G= GRCh37
NC_000002.10:g.219633164G= NCBI36
NG_016741.1:g.5319C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.270C= MANE Select ENSP00000295731.5:p.Ile90=
ENST00000295731.6:c.270C= ENSP00000295731.5:p.Ile90=
NM_002181.3:c.270C= NP_002172.2:p.Ile90=
NM_002181.4:c.270C= MANE Select NP_002172.2:p.Ile90=