Canonical Allele Identifier: CA357620624
Gene: IBSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811440A>T , CM000666.2:g.87811440A>T GRCh38
NC_000004.11:g.88732592A>T , CM000666.1:g.88732592A>T GRCh37
NC_000004.10:g.88951616A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.484A>T MANE Select ENSP00000226284.5:p.Asn162Tyr
ENST00000226284.6:c.484A>T ENSP00000226284.5:p.Asn162Tyr
NM_004967.3:c.484A>T NP_004958.2:p.Asn162Tyr
NM_004967.4:c.484A>T MANE Select NP_004958.2:p.Asn162Tyr