Canonical Allele Identifier: CA3002400
Gene: IBSP HGNC NCBI

Linked Data

dbSNP Id: rs768315657
gnomAD v2: 4-88732600-A-C
gnomAD v4: 4-87811448-A-C

Genomic Alleles

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

Transcript Alleles

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