Canonical Allele Identifier: CA440295364
Gene: IBSP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88732516T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811364T>C , CM000666.2:g.87811364T>C GRCh38
NC_000004.11:g.88732516T>C , CM000666.1:g.88732516T>C GRCh37
NC_000004.10:g.88951540T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.408T>C MANE Select ENSP00000226284.5:p.Ala136=
ENST00000226284.6:c.408T>C ENSP00000226284.5:p.Ala136=
NM_004967.3:c.408T>C NP_004958.2:p.Ala136=
NM_004967.4:c.408T>C MANE Select NP_004958.2:p.Ala136=
Search 100 bp 5'
Search 100 bp 3'