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Canonical Allele Identifier:
CA1329042574
Community Standard Title: NM_002181.4(IHH):c.298G= (p.Asp100=)
Gene: IHH
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.219060170C= , CM000664.2:g.219060170C=
GRCh38
NC_000002.11:g.219924892C= , CM000664.1:g.219924892C=
GRCh37
NC_000002.10:g.219633136C=
NCBI36
NG_016741.1:g.5347G=
Transcript Alleles
HGVS
Amino-acid Change
NM_002181.4:c.298G=
MANE Select
NP_002172.2:p.Asp100=
ENST00000295731.7:c.298G=
MANE Select
ENSP00000295731.5:p.Asp100=
NM_002181.3:c.298G=
NP_002172.2:p.Asp100=
ENST00000295731.6:c.298G=
ENSP00000295731.5:p.Asp100=
Search 100 bp 5'
Search 100 bp 3'