Canonical Allele Identifier: CA1329042723
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060477G= , CM000664.2:g.219060477G= GRCh38
NC_000002.11:g.219925199G= , CM000664.1:g.219925199G= GRCh37
NC_000002.10:g.219633443G= NCBI36
NG_016741.1:g.5040C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-10C= MANE Select ENSP00000295731.5:n.-10C=
NM_002181.3:c.-10C= NP_002172.2:n.-10C=
NM_002181.4:c.-10C= MANE Select NP_002172.2:n.-10C=