Canonical Allele Identifier: CA1474474546
Gene: IBSP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811343T= , CM000666.2:g.87811343T= GRCh38
NC_000004.11:g.88732495T= , CM000666.1:g.88732495T= GRCh37
NC_000004.10:g.88951519T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.406-19T= MANE Select ENSP00000226284.5:n.406-19T=
ENST00000226284.6:c.406-19T= ENSP00000226284.5:n.406-19T=
NM_004967.3:c.406-19T= NP_004958.2:n.406-19T=
NM_004967.4:c.406-19T= MANE Select NP_004958.2:n.406-19T=
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