Canonical Allele Identifier: CA357621016
Gene: IBSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811540G>T , CM000666.2:g.87811540G>T GRCh38
NC_000004.11:g.88732692G>T , CM000666.1:g.88732692G>T GRCh37
NC_000004.10:g.88951716G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.584G>T MANE Select ENSP00000226284.5:p.Gly195Val
ENST00000226284.6:c.584G>T ENSP00000226284.5:p.Gly195Val
NM_004967.3:c.584G>T NP_004958.2:p.Gly195Val
NM_004967.4:c.584G>T MANE Select NP_004958.2:p.Gly195Val