Canonical Allele Identifier: CA1042494157
Gene: IHH HGNC NCBI

Linked Data

gnomAD v3: 2-219060507-G-C
gnomAD v4: 2-219060507-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060507G>C , CM000664.2:g.219060507G>C GRCh38
NC_000002.11:g.219925229G>C , CM000664.1:g.219925229G>C GRCh37
NC_000002.10:g.219633473G>C NCBI36
NG_016741.1:g.5010C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-40C>G MANE Select ENSP00000295731.5:n.-40C>G
NM_002181.3:c.-40C>G NP_002172.2:n.-40C>G
NM_002181.4:c.-40C>G MANE Select NP_002172.2:n.-40C>G
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