Canonical Allele Identifier: CA1329042774
Gene: IHH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060548G= , CM000664.2:g.219060548G= GRCh38
NC_000002.11:g.219925270G= , CM000664.1:g.219925270G= GRCh37
NC_000002.10:g.219633514G= NCBI36
NG_016741.1:g.4969C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-81C= MANE Select ENSP00000295731.5:n.-81C=
NM_002181.4:c.-81C= MANE Select NP_002172.2:n.-81C=
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