Canonical Allele Identifier: CA471739198

Gene: BAG3

Linked Data

• ClinVar Variation Id: 936070
• ClinVar RCV Id: RCV001204793
• dbSNP Id: rs1384999606
• MyVariant Identifiers: chr10:g.121431835C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672323C>T , CM000672.2:g.119672323C>T	GRCh38
NC_000010.10:g.121431835C>T , CM000672.1:g.121431835C>T	GRCh37
NC_000010.9:g.121421825C>T	NCBI36
NG_016125.1:g.25954C>T , LRG_742:g.25954C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.576C>T MANE Select	ENSP00000358081.4:p.Gly192=
ENST00000369085.7:c.576C>T	ENSP00000358081.3:p.Gly192=
ENST00000450186.1:c.402C>T	ENSP00000410036.1:p.Gly134=
NM_004281.3:c.576C>T , LRG_742t1:c.576C>T	NP_004272.2:p.Gly192=
XM_005270287.1:c.576C>T	XP_005270344.1:p.Gly192=
XM_005270287.2:c.576C>T	XP_005270344.1:p.Gly192=
NM_004281.4:c.576C>T MANE Select	NP_004272.2:p.Gly192=