Canonical Allele Identifier: CA1329042586
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060187T= , CM000664.2:g.219060187T= GRCh38
NC_000002.11:g.219924909T= , CM000664.1:g.219924909T= GRCh37
NC_000002.10:g.219633153T= NCBI36
NG_016741.1:g.5330A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.281A= MANE Select ENSP00000295731.5:p.Glu94=
ENST00000295731.6:c.281A= ENSP00000295731.5:p.Glu94=
NM_002181.3:c.281A= NP_002172.2:p.Glu94=
NM_002181.4:c.281A= MANE Select NP_002172.2:p.Glu94=