Canonical Allele Identifier: CA350636728
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219924913C>T (hg19) chr2:g.219060191C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060191C>T , CM000664.2:g.219060191C>T GRCh38
NC_000002.11:g.219924913C>T , CM000664.1:g.219924913C>T GRCh37
NC_000002.10:g.219633157C>T NCBI36
NG_016741.1:g.5326G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.277G>A MANE Select ENSP00000295731.5:p.Asp93Asn
ENST00000295731.6:c.277G>A ENSP00000295731.5:p.Asp93Asn
NM_002181.3:c.277G>A NP_002172.2:p.Asp93Asn
NM_002181.4:c.277G>A MANE Select NP_002172.2:p.Asp93Asn
Search 100 bp 5'
Search 100 bp 3'