Canonical Allele Identifier: CA1329042768
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs961103388
gnomAD v4: 2-219060533-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060533G>T , CM000664.2:g.219060533G>T GRCh38
NC_000002.11:g.219925255G>T , CM000664.1:g.219925255G>T GRCh37
NC_000002.10:g.219633499G>T NCBI36
NG_016741.1:g.4984C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-66C>A MANE Select ENSP00000295731.5:n.-66C>A
NM_002181.4:c.-66C>A MANE Select NP_002172.2:n.-66C>A
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