Canonical Allele Identifier: CA1474474595
Gene: IBSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811457A= , CM000666.2:g.87811457A= GRCh38
NC_000004.11:g.88732609A= , CM000666.1:g.88732609A= GRCh37
NC_000004.10:g.88951633A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000226284.7:c.501A= MANE Select ENSP00000226284.5:p.Ala167=
ENST00000226284.6:c.501A= ENSP00000226284.5:p.Ala167=
NM_004967.3:c.501A= NP_004958.2:p.Ala167=
NM_004967.4:c.501A= MANE Select NP_004958.2:p.Ala167=