Canonical Allele Identifier: CA2577248553
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060089-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060089G>T , CM000664.2:g.219060089G>T GRCh38
NC_000002.11:g.219924811G>T , CM000664.1:g.219924811G>T GRCh37
NC_000002.10:g.219633055G>T NCBI36
NG_016741.1:g.5428C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.315+64C>A MANE Select ENSP00000295731.5:n.315+64C>A
ENST00000295731.6:c.315+64C>A ENSP00000295731.5:n.315+64C>A
NM_002181.3:c.315+64C>A NP_002172.2:n.315+64C>A
NM_002181.4:c.315+64C>A MANE Select NP_002172.2:n.315+64C>A
Search 100 bp 5'
Search 100 bp 3'