Canonical Allele Identifier: CA553085741
Gene: IBSP HGNC NCBI

Linked Data

dbSNP Id: rs1317267943

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811555_87811557del , CM000666.2:g.87811555_87811557del GRCh38
NC_000004.11:g.88732707_88732709del , CM000666.1:g.88732707_88732709del GRCh37
NC_000004.10:g.88951731_88951733del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.599_601del MANE Select ENSP00000226284.5:p.Glu200del
ENST00000226284.6:c.599_601del ENSP00000226284.5:p.Glu200del
NM_004967.3:c.599_601del NP_004958.2:p.Glu200del
NM_004967.4:c.599_601del MANE Select NP_004958.2:p.Glu200del