Canonical Allele Identifier: CA350637545
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219925099C>T (hg19) chr2:g.219060377C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060377C>T , CM000664.2:g.219060377C>T GRCh38
NC_000002.11:g.219925099C>T , CM000664.1:g.219925099C>T GRCh37
NC_000002.10:g.219633343C>T NCBI36
NG_016741.1:g.5140G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.91G>A MANE Select ENSP00000295731.5:p.Gly31Ser
ENST00000295731.6:c.91G>A ENSP00000295731.5:p.Gly31Ser
NM_002181.3:c.91G>A NP_002172.2:p.Gly31Ser
NM_002181.4:c.91G>A MANE Select NP_002172.2:p.Gly31Ser
Search 100 bp 5'
Search 100 bp 3'