Canonical Allele Identifier: CA1474474555
Gene: IBSP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811365G= , CM000666.2:g.87811365G= GRCh38
NC_000004.11:g.88732517G= , CM000666.1:g.88732517G= GRCh37
NC_000004.10:g.88951541G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.409G= MANE Select ENSP00000226284.5:p.Gly137=
ENST00000226284.6:c.409G= ENSP00000226284.5:p.Gly137=
NM_004967.3:c.409G= NP_004958.2:p.Gly137=
NM_004967.4:c.409G= MANE Select NP_004958.2:p.Gly137=
Search 100 bp 5'
Search 100 bp 3'