Canonical Allele Identifier: CA350637725
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219925153A>T (hg19) chr2:g.219060431A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060431A>T , CM000664.2:g.219060431A>T GRCh38
NC_000002.11:g.219925153A>T , CM000664.1:g.219925153A>T GRCh37
NC_000002.10:g.219633397A>T NCBI36
NG_016741.1:g.5086T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.37T>A MANE Select ENSP00000295731.5:p.Cys13Ser
ENST00000295731.6:c.37T>A ENSP00000295731.5:p.Cys13Ser
NM_002181.3:c.37T>A NP_002172.2:p.Cys13Ser
NM_002181.4:c.37T>A MANE Select NP_002172.2:p.Cys13Ser
Search 100 bp 5'
Search 100 bp 3'