Canonical Allele Identifier: CA1329042722
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060475G= , CM000664.2:g.219060475G= GRCh38
NC_000002.11:g.219925197G= , CM000664.1:g.219925197G= GRCh37
NC_000002.10:g.219633441G= NCBI36
NG_016741.1:g.5042C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-8C= MANE Select ENSP00000295731.5:n.-8C=
NM_002181.3:c.-8C= NP_002172.2:n.-8C=
NM_002181.4:c.-8C= MANE Select NP_002172.2:n.-8C=