Canonical Allele Identifier: CA2663195396
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060557-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060557T>C , CM000664.2:g.219060557T>C GRCh38
NC_000002.11:g.219925279T>C , CM000664.1:g.219925279T>C GRCh37
NC_000002.10:g.219633523T>C NCBI36
NG_016741.1:g.4960A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-90A>G MANE Select ENSP00000295731.5:n.-90A>G
NM_002181.4:c.-90A>G MANE Select NP_002172.2:n.-90A>G
Search 100 bp 5'
Search 100 bp 3'