Canonical Allele Identifier: CA1329042762
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060528T= , CM000664.2:g.219060528T= GRCh38
NC_000002.11:g.219925250T= , CM000664.1:g.219925250T= GRCh37
NC_000002.10:g.219633494T= NCBI36
NG_016741.1:g.4989A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-61A= MANE Select ENSP00000295731.5:n.-61A=
NM_002181.4:c.-61A= MANE Select NP_002172.2:n.-61A=