Canonical Allele Identifier: CA1474474552
Gene: IBSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811355C= , CM000666.2:g.87811355C= GRCh38
NC_000004.11:g.88732507C= , CM000666.1:g.88732507C= GRCh37
NC_000004.10:g.88951531C= NCBI36

Transcript Alleles

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