Canonical Allele Identifier: CA440295859
Gene: IBSP HGNC NCBI

Linked Data

dbSNP Id: rs767350101
MyVariant Identifiers: chr4:g.88732693A>G (hg19)

Genomic Alleles

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

Transcript Alleles

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