Canonical Allele Identifier: CA539841245
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs1192800287
gnomAD v2: 2-219925202-CG-C
gnomAD v4: 2-219060480-CG-C
MyVariant Identifiers: chr2:g.219925203del (hg19) chr2:g.219060481del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060485del , CM000664.2:g.219060485del GRCh38
NC_000002.11:g.219925207del , CM000664.1:g.219925207del GRCh37
NC_000002.10:g.219633451del NCBI36
NG_016741.1:g.5036del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-14del MANE Select ENSP00000295731.5:n.-14del
NM_002181.3:c.-14del NP_002172.2:n.-14del
NM_002181.4:c.-14del MANE Select NP_002172.2:n.-14del
Search 100 bp 5'
Search 100 bp 3'