Canonical Allele Identifier: CA357620625

Gene: IBSP

Linked Data

• MyVariant Identifiers: chr4:g.88732593A>C (hg19) ; chr4:g.87811441A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000226284.7:c.485A>C MANE Select	ENSP00000226284.5:p.Asn162Thr
ENST00000226284.6:c.485A>C	ENSP00000226284.5:p.Asn162Thr
NM_004967.3:c.485A>C	NP_004958.2:p.Asn162Thr
NM_004967.4:c.485A>C MANE Select	NP_004958.2:p.Asn162Thr