Canonical Allele Identifier: CA2663195342
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060515-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060515A>G , CM000664.2:g.219060515A>G GRCh38
NC_000002.11:g.219925237A>G , CM000664.1:g.219925237A>G GRCh37
NC_000002.10:g.219633481A>G NCBI36
NG_016741.1:g.5002T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-48T>C MANE Select ENSP00000295731.5:n.-48T>C
NM_002181.3:c.-48T>C NP_002172.2:n.-48T>C
NM_002181.4:c.-48T>C MANE Select NP_002172.2:n.-48T>C
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