Canonical Allele Identifier: CA357620646
Gene: IBSP HGNC NCBI

Linked Data

dbSNP Id: rs1222510068
gnomAD v2: 4-88732598-G-C
gnomAD v3: 4-87811446-G-C
gnomAD v4: 4-87811446-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811446G>C , CM000666.2:g.87811446G>C GRCh38
NC_000004.11:g.88732598G>C , CM000666.1:g.88732598G>C GRCh37
NC_000004.10:g.88951622G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.490G>C MANE Select ENSP00000226284.5:p.Glu164Gln
ENST00000226284.6:c.490G>C ENSP00000226284.5:p.Glu164Gln
NM_004967.3:c.490G>C NP_004958.2:p.Glu164Gln
NM_004967.4:c.490G>C MANE Select NP_004958.2:p.Glu164Gln