Canonical Allele Identifier: CA471740278
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2951832
ClinVar RCV Id: RCV003812519
MyVariant Identifiers: chr10:g.121432105G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672593G>A , CM000672.2:g.119672593G>A GRCh38
NC_000010.10:g.121432105G>A , CM000672.1:g.121432105G>A GRCh37
NC_000010.9:g.121422095G>A NCBI36
NG_016125.1:g.26224G>A , LRG_742:g.26224G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.846G>A MANE Select ENSP00000358081.4:p.Arg282=
ENST00000369085.7:c.846G>A ENSP00000358081.3:p.Arg282=
ENST00000450186.1:c.672G>A ENSP00000410036.1:p.Arg224=
NM_004281.3:c.846G>A , LRG_742t1:c.846G>A NP_004272.2:p.Arg282=
XM_005270287.1:c.846G>A XP_005270344.1:p.Arg282=
XM_005270287.2:c.846G>A XP_005270344.1:p.Arg282=
NM_004281.4:c.846G>A MANE Select NP_004272.2:p.Arg282=
Search 100 bp 5'
Search 100 bp 3'