Canonical Allele Identifier: CA1474474548
Gene: IBSP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811349C= , CM000666.2:g.87811349C= GRCh38
NC_000004.11:g.88732501C= , CM000666.1:g.88732501C= GRCh37
NC_000004.10:g.88951525C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.406-13C= MANE Select ENSP00000226284.5:n.406-13C=
ENST00000226284.6:c.406-13C= ENSP00000226284.5:n.406-13C=
NM_004967.3:c.406-13C= NP_004958.2:n.406-13C=
NM_004967.4:c.406-13C= MANE Select NP_004958.2:n.406-13C=
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