Canonical Allele Identifier: CA357620626
Gene: IBSP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88732593A>G (hg19) chr4:g.87811441A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811441A>G , CM000666.2:g.87811441A>G GRCh38
NC_000004.11:g.88732593A>G , CM000666.1:g.88732593A>G GRCh37
NC_000004.10:g.88951617A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.485A>G MANE Select ENSP00000226284.5:p.Asn162Ser
ENST00000226284.6:c.485A>G ENSP00000226284.5:p.Asn162Ser
NM_004967.3:c.485A>G NP_004958.2:p.Asn162Ser
NM_004967.4:c.485A>G MANE Select NP_004958.2:p.Asn162Ser
Search 100 bp 5'
Search 100 bp 3'