Canonical Allele Identifier: CA1329042668
Gene: IHH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060374G= , CM000664.2:g.219060374G= GRCh38
NC_000002.11:g.219925096G= , CM000664.1:g.219925096G= GRCh37
NC_000002.10:g.219633340G= NCBI36
NG_016741.1:g.5143C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.94C= MANE Select ENSP00000295731.5:p.Arg32=
ENST00000295731.6:c.94C= ENSP00000295731.5:p.Arg32=
NM_002181.3:c.94C= NP_002172.2:p.Arg32=
NM_002181.4:c.94C= MANE Select NP_002172.2:p.Arg32=
Search 100 bp 5'
Search 100 bp 3'