Canonical Allele Identifier: CA1329042589
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060196A= , CM000664.2:g.219060196A= GRCh38
NC_000002.11:g.219924918A= , CM000664.1:g.219924918A= GRCh37
NC_000002.10:g.219633162A= NCBI36
NG_016741.1:g.5321T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.272T= MANE Select ENSP00000295731.5:p.Phe91=
ENST00000295731.6:c.272T= ENSP00000295731.5:p.Phe91=
NM_002181.3:c.272T= NP_002172.2:p.Phe91=
NM_002181.4:c.272T= MANE Select NP_002172.2:p.Phe91=