Canonical Allele Identifier: CA2663195397
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060558-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060558C>A , CM000664.2:g.219060558C>A GRCh38
NC_000002.11:g.219925280C>A , CM000664.1:g.219925280C>A GRCh37
NC_000002.10:g.219633524C>A NCBI36
NG_016741.1:g.4959G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-91G>T MANE Select ENSP00000295731.5:n.-91G>T
NM_002181.4:c.-91G>T MANE Select NP_002172.2:n.-91G>T
Search 100 bp 5'
Search 100 bp 3'