Canonical Allele Identifier: CA357620672
Gene: IBSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811453A>G , CM000666.2:g.87811453A>G GRCh38
NC_000004.11:g.88732605A>G , CM000666.1:g.88732605A>G GRCh37
NC_000004.10:g.88951629A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.497A>G MANE Select ENSP00000226284.5:p.Glu166Gly
ENST00000226284.6:c.497A>G ENSP00000226284.5:p.Glu166Gly
NM_004967.3:c.497A>G NP_004958.2:p.Glu166Gly
NM_004967.4:c.497A>G MANE Select NP_004958.2:p.Glu166Gly