Canonical Allele Identifier: CA289665

Gene: BAG3

Linked Data

• ClinVar Variation Id: 136494
• ClinVar RCV Id: RCV000123818 ; RCV000317614 ; RCV000372291
• dbSNP Id: rs200388926
• ExAC: 10:121411171 G / A
• gnomAD v2: 10-121411171-G-A
• gnomAD v3: 10-119651659-G-A
• gnomAD v4: 10-119651659-G-A
• MyVariant Identifiers: chr10:g.121411171G>A (hg19) ; chr10:g.119651659G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119651659G>A , CM000672.2:g.119651659G>A	GRCh38
NC_000010.10:g.121411171G>A , CM000672.1:g.121411171G>A	GRCh37
NC_000010.9:g.121401161G>A	NCBI36
NG_016125.1:g.5290G>A , LRG_742:g.5290G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369085.8:c.-17G>A MANE Select	ENSP00000358081.4:n.-17G>A
ENST00000369085.7:c.-17G>A	ENSP00000358081.3:n.-17G>A
NM_004281.3:c.-17G>A , LRG_742t1:c.-17G>A	NP_004272.2:n.-17G>A
XM_005270287.1:c.-17G>A	XP_005270344.1:n.-17G>A
XM_005270287.2:c.-17G>A	XP_005270344.1:n.-17G>A
NM_004281.4:c.-17G>A MANE Select	NP_004272.2:n.-17G>A