Canonical Allele Identifier: CA357621019
Gene: IBSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811542G>C , CM000666.2:g.87811542G>C GRCh38
NC_000004.11:g.88732694G>C , CM000666.1:g.88732694G>C GRCh37
NC_000004.10:g.88951718G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.586G>C MANE Select ENSP00000226284.5:p.Asp196His
ENST00000226284.6:c.586G>C ENSP00000226284.5:p.Asp196His
NM_004967.3:c.586G>C NP_004958.2:p.Asp196His
NM_004967.4:c.586G>C MANE Select NP_004958.2:p.Asp196His