Canonical Allele Identifier: CA1329042585
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060186C= , CM000664.2:g.219060186C= GRCh38
NC_000002.11:g.219924908C= , CM000664.1:g.219924908C= GRCh37
NC_000002.10:g.219633152C= NCBI36
NG_016741.1:g.5331G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.282G= MANE Select ENSP00000295731.5:p.Glu94=
ENST00000295731.6:c.282G= ENSP00000295731.5:p.Glu94=
NM_002181.3:c.282G= NP_002172.2:p.Glu94=
NM_002181.4:c.282G= MANE Select NP_002172.2:p.Glu94=