Canonical Allele Identifier: CA1329042512
Gene: IHH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060080C= , CM000664.2:g.219060080C= GRCh38
NC_000002.11:g.219924802C= , CM000664.1:g.219924802C= GRCh37
NC_000002.10:g.219633046C= NCBI36
NG_016741.1:g.5437G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.315+73G= MANE Select ENSP00000295731.5:n.315+73G=
ENST00000295731.6:c.315+73G= ENSP00000295731.5:n.315+73G=
NM_002181.3:c.315+73G= NP_002172.2:n.315+73G=
NM_002181.4:c.315+73G= MANE Select NP_002172.2:n.315+73G=
Search 100 bp 5'
Search 100 bp 3'