Canonical Allele Identifier: CA1329042667
Gene: IHH HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060373C= , CM000664.2:g.219060373C= GRCh38
NC_000002.11:g.219925095C= , CM000664.1:g.219925095C= GRCh37
NC_000002.10:g.219633339C= NCBI36
NG_016741.1:g.5144G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.95G= MANE Select ENSP00000295731.5:p.Arg32=
ENST00000295731.6:c.95G= ENSP00000295731.5:p.Arg32=
NM_002181.3:c.95G= NP_002172.2:p.Arg32=
NM_002181.4:c.95G= MANE Select NP_002172.2:p.Arg32=
Search 100 bp 5'
Search 100 bp 3'