Canonical Allele Identifier: CA2663195328
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060505-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060505T>C , CM000664.2:g.219060505T>C GRCh38
NC_000002.11:g.219925227T>C , CM000664.1:g.219925227T>C GRCh37
NC_000002.10:g.219633471T>C NCBI36
NG_016741.1:g.5012A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-38A>G MANE Select ENSP00000295731.5:n.-38A>G
NM_002181.3:c.-38A>G NP_002172.2:n.-38A>G
NM_002181.4:c.-38A>G MANE Select NP_002172.2:n.-38A>G
Search 100 bp 5'
Search 100 bp 3'