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ClinGen Allele Registry
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Canonical Allele Identifier:
CA1329042583
Community Standard Title: NM_002181.4(IHH):c.284A= (p.Glu95=)
Gene: IHH
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.219060184T= , CM000664.2:g.219060184T=
GRCh38
NC_000002.11:g.219924906T= , CM000664.1:g.219924906T=
GRCh37
NC_000002.10:g.219633150T=
NCBI36
NG_016741.1:g.5333A=
Transcript Alleles
HGVS
Amino-acid Change
NM_002181.4:c.284A=
MANE Select
NP_002172.2:p.Glu95=
ENST00000295731.7:c.284A=
MANE Select
ENSP00000295731.5:p.Glu95=
NM_002181.3:c.284A=
NP_002172.2:p.Glu95=
ENST00000295731.6:c.284A=
ENSP00000295731.5:p.Glu95=
Search 100 bp 5'
Search 100 bp 3'