Canonical Allele Identifier: CA350637161
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219925023A>C (hg19) chr2:g.219060301A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060301A>C , CM000664.2:g.219060301A>C GRCh38
NC_000002.11:g.219925023A>C , CM000664.1:g.219925023A>C GRCh37
NC_000002.10:g.219633267A>C NCBI36
NG_016741.1:g.5216T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.167T>G MANE Select ENSP00000295731.5:p.Val56Gly
ENST00000295731.6:c.167T>G ENSP00000295731.5:p.Val56Gly
NM_002181.3:c.167T>G NP_002172.2:p.Val56Gly
NM_002181.4:c.167T>G MANE Select NP_002172.2:p.Val56Gly
Search 100 bp 5'
Search 100 bp 3'