Canonical Allele Identifier: CA378294756
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449416
ClinVar RCV Id: RCV002004598
dbSNP Id: rs1236900746
MyVariant Identifiers: chr10:g.121429448T>A (hg19) chr10:g.119669936T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669936T>A , CM000672.2:g.119669936T>A GRCh38
NC_000010.10:g.121429448T>A , CM000672.1:g.121429448T>A GRCh37
NC_000010.9:g.121419438T>A NCBI36
NG_016125.1:g.23567T>A , LRG_742:g.23567T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.266T>A MANE Select ENSP00000358081.4:p.Leu89His
ENST00000369085.7:c.266T>A ENSP00000358081.3:p.Leu89His
ENST00000450186.1:c.92T>A ENSP00000410036.1:p.Leu31His
NM_004281.3:c.266T>A , LRG_742t1:c.266T>A NP_004272.2:p.Leu89His
XM_005270287.1:c.266T>A XP_005270344.1:p.Leu89His
XM_005270287.2:c.266T>A XP_005270344.1:p.Leu89His
NM_004281.4:c.266T>A MANE Select NP_004272.2:p.Leu89His
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Search 100 bp 3'