Canonical Allele Identifier: CA2663195407
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060563-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060563T>G , CM000664.2:g.219060563T>G GRCh38
NC_000002.11:g.219925285T>G , CM000664.1:g.219925285T>G GRCh37
NC_000002.10:g.219633529T>G NCBI36
NG_016741.1:g.4954A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-96A>C MANE Select ENSP00000295731.5:n.-96A>C
NM_002181.4:c.-96A>C MANE Select NP_002172.2:n.-96A>C
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