Canonical Allele Identifier: CA1474474635
Gene: IBSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811543A= , CM000666.2:g.87811543A= GRCh38
NC_000004.11:g.88732695A= , CM000666.1:g.88732695A= GRCh37
NC_000004.10:g.88951719A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.587A= MANE Select ENSP00000226284.5:p.Asp196=
ENST00000226284.6:c.587A= ENSP00000226284.5:p.Asp196=
NM_004967.3:c.587A= NP_004958.2:p.Asp196=
NM_004967.4:c.587A= MANE Select NP_004958.2:p.Asp196=