Canonical Allele Identifier: CA431420226
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs1948869488
COSMIC: COSM3044401
MyVariant Identifiers: chr2:g.219925025A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060303A>G , CM000664.2:g.219060303A>G GRCh38
NC_000002.11:g.219925025A>G , CM000664.1:g.219925025A>G GRCh37
NC_000002.10:g.219633269A>G NCBI36
NG_016741.1:g.5214T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.165T>C MANE Select ENSP00000295731.5:p.Asn55=
ENST00000295731.6:c.165T>C ENSP00000295731.5:p.Asn55=
NM_002181.3:c.165T>C NP_002172.2:p.Asn55=
NM_002181.4:c.165T>C MANE Select NP_002172.2:p.Asn55=
Search 100 bp 5'
Search 100 bp 3'