Canonical Allele Identifier: CA378296277

Gene: BAG3

Linked Data

• ClinVar Variation Id: 1177802
• ClinVar RCV Id: RCV001533960
• dbSNP Id: rs869248137
• MyVariant Identifiers: chr10:g.121435991C>G (hg19) ; chr10:g.119676479C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119676479C>G , CM000672.2:g.119676479C>G	GRCh38
NC_000010.10:g.121435991C>G , CM000672.1:g.121435991C>G	GRCh37
NC_000010.9:g.121425981C>G	NCBI36
NG_016125.1:g.30110C>G , LRG_742:g.30110C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369085.8:c.925C>G MANE Select	ENSP00000358081.4:p.Arg309Gly
ENST00000369085.7:c.925C>G	ENSP00000358081.3:p.Arg309Gly
ENST00000450186.1:c.748C>G	ENSP00000410036.1:p.Arg250Gly
NM_004281.3:c.925C>G , LRG_742t1:c.925C>G	NP_004272.2:p.Arg309Gly
XM_005270287.1:c.922C>G	XP_005270344.1:p.Arg308Gly
XM_005270287.2:c.922C>G	XP_005270344.1:p.Arg308Gly
NM_004281.4:c.925C>G MANE Select	NP_004272.2:p.Arg309Gly