Canonical Allele Identifier: CA764946678
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs1398894592
gnomAD v4: 2-219060583-C-A
MyVariant Identifiers: chr2:g.219925305C>A (hg19) chr2:g.219060583C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060583C>A , CM000664.2:g.219060583C>A GRCh38
NC_000002.11:g.219925305C>A , CM000664.1:g.219925305C>A GRCh37
NC_000002.10:g.219633549C>A NCBI36
NG_016741.1:g.4934G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-116G>T MANE Select ENSP00000295731.5:n.-116G>T
NM_002181.4:c.-116G>T MANE Select NP_002172.2:n.-116G>T
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Search 100 bp 3'