Canonical Allele Identifier: CA440295368
Gene: IBSP HGNC NCBI

Linked Data

COSMIC: COSM5023443
MyVariant Identifiers: chr4:g.88732519G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811367G>T , CM000666.2:g.87811367G>T GRCh38
NC_000004.11:g.88732519G>T , CM000666.1:g.88732519G>T GRCh37
NC_000004.10:g.88951543G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000226284.7:c.411G>T MANE Select ENSP00000226284.5:p.Gly137=
ENST00000226284.6:c.411G>T ENSP00000226284.5:p.Gly137=
NM_004967.3:c.411G>T NP_004958.2:p.Gly137=
NM_004967.4:c.411G>T MANE Select NP_004958.2:p.Gly137=
Search 100 bp 5'
Search 100 bp 3'