Canonical Allele Identifier: CA65951302
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs867033547

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060314A>G , CM000664.2:g.219060314A>G GRCh38
NC_000002.11:g.219925036A>G , CM000664.1:g.219925036A>G GRCh37
NC_000002.10:g.219633280A>G NCBI36
NG_016741.1:g.5203T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.154T>C MANE Select ENSP00000295731.5:p.Phe52Leu
ENST00000295731.6:c.154T>C ENSP00000295731.5:p.Phe52Leu
NM_002181.3:c.154T>C NP_002172.2:p.Phe52Leu
NM_002181.4:c.154T>C MANE Select NP_002172.2:p.Phe52Leu