Canonical Allele Identifier: CA2663195370
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060541-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060541T>C , CM000664.2:g.219060541T>C GRCh38
NC_000002.11:g.219925263T>C , CM000664.1:g.219925263T>C GRCh37
NC_000002.10:g.219633507T>C NCBI36
NG_016741.1:g.4976A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-74A>G MANE Select ENSP00000295731.5:n.-74A>G
NM_002181.4:c.-74A>G MANE Select NP_002172.2:n.-74A>G
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