Canonical Allele Identifier: CA135037

Gene: BAG3

Linked Data

• ClinVar Variation Id: 44791
• ClinVar RCV Id: RCV000037901 ; RCV000538221 ; RCV000619465 ; RCV003333952 ; RCV003952431
• dbSNP Id: rs140737221
• ExAC: 10:121432129 C / G
• gnomAD v2: 10-121432129-C-G
• gnomAD v3: 10-119672617-C-G
• gnomAD v4: 10-119672617-C-G
• MyVariant Identifiers: chr10:g.121432129C>G (hg19) ; chr10:g.119672617C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672617C>G , CM000672.2:g.119672617C>G	GRCh38
NC_000010.10:g.121432129C>G , CM000672.1:g.121432129C>G	GRCh37
NC_000010.9:g.121422119C>G	NCBI36
NG_016125.1:g.26248C>G , LRG_742:g.26248C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.870C>G MANE Select	ENSP00000358081.4:p.Pro290=
ENST00000369085.7:c.870C>G	ENSP00000358081.3:p.Pro290=
ENST00000450186.1:c.696C>G	ENSP00000410036.1:p.Pro232=
NM_004281.3:c.870C>G , LRG_742t1:c.870C>G	NP_004272.2:p.Pro290=
XM_005270287.1:c.870C>G	XP_005270344.1:p.Pro290=
XM_005270287.2:c.870C>G	XP_005270344.1:p.Pro290=
NM_004281.4:c.870C>G MANE Select	NP_004272.2:p.Pro290=