Canonical Allele Identifier: CA3002429
Gene: IBSP HGNC NCBI

Linked Data

dbSNP Id: rs767350101
gnomAD v2: 4-88732693-A-T
gnomAD v4: 4-87811541-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811541A>T , CM000666.2:g.87811541A>T GRCh38
NC_000004.11:g.88732693A>T , CM000666.1:g.88732693A>T GRCh37
NC_000004.10:g.88951717A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.585A>T MANE Select ENSP00000226284.5:p.Gly195=
ENST00000226284.6:c.585A>T ENSP00000226284.5:p.Gly195=
NM_004967.3:c.585A>T NP_004958.2:p.Gly195=
NM_004967.4:c.585A>T MANE Select NP_004958.2:p.Gly195=