Canonical Allele Identifier: CA65951406
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs1042787562

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060395C>A , CM000664.2:g.219060395C>A GRCh38
NC_000002.11:g.219925117C>A , CM000664.1:g.219925117C>A GRCh37
NC_000002.10:g.219633361C>A NCBI36
NG_016741.1:g.5122G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.73G>T MANE Select ENSP00000295731.5:p.Ala25Ser
ENST00000295731.6:c.73G>T ENSP00000295731.5:p.Ala25Ser
NM_002181.3:c.73G>T NP_002172.2:p.Ala25Ser
NM_002181.4:c.73G>T MANE Select NP_002172.2:p.Ala25Ser