Canonical Allele Identifier: CA1329042729
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060483G= , CM000664.2:g.219060483G= GRCh38
NC_000002.11:g.219925205G= , CM000664.1:g.219925205G= GRCh37
NC_000002.10:g.219633449G= NCBI36
NG_016741.1:g.5034C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-16C= MANE Select ENSP00000295731.5:n.-16C=
NM_002181.3:c.-16C= NP_002172.2:n.-16C=
NM_002181.4:c.-16C= MANE Select NP_002172.2:n.-16C=