Canonical Allele Identifier: CA357620622
Gene: IBSP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.484A>G MANE Select ENSP00000226284.5:p.Asn162Asp
ENST00000226284.6:c.484A>G ENSP00000226284.5:p.Asn162Asp
NM_004967.3:c.484A>G NP_004958.2:p.Asn162Asp
NM_004967.4:c.484A>G MANE Select NP_004958.2:p.Asn162Asp