Canonical Allele Identifier: CA357620654
Gene: IBSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811448A>T , CM000666.2:g.87811448A>T GRCh38
NC_000004.11:g.88732600A>T , CM000666.1:g.88732600A>T GRCh37
NC_000004.10:g.88951624A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.492A>T MANE Select ENSP00000226284.5:p.Glu164Asp
ENST00000226284.6:c.492A>T ENSP00000226284.5:p.Glu164Asp
NM_004967.3:c.492A>T NP_004958.2:p.Glu164Asp
NM_004967.4:c.492A>T MANE Select NP_004958.2:p.Glu164Asp