Canonical Allele Identifier: CA5716416
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 508170
ClinVar RCV Id: RCV000648851 RCV001722633 RCV002431771
dbSNP Id: rs776700820
ExAC: 10:121432081 G / A
gnomAD v2: 10-121432081-G-A
gnomAD v3: 10-119672569-G-A
gnomAD v4: 10-119672569-G-A
MyVariant Identifiers: chr10:g.121432081G>A (hg19) chr10:g.119672569G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672569G>A , CM000672.2:g.119672569G>A GRCh38
NC_000010.10:g.121432081G>A , CM000672.1:g.121432081G>A GRCh37
NC_000010.9:g.121422071G>A NCBI36
NG_016125.1:g.26200G>A , LRG_742:g.26200G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.822G>A MANE Select ENSP00000358081.4:p.Ser274=
ENST00000369085.7:c.822G>A ENSP00000358081.3:p.Ser274=
ENST00000450186.1:c.648G>A ENSP00000410036.1:p.Ser216=
NM_004281.3:c.822G>A , LRG_742t1:c.822G>A NP_004272.2:p.Ser274=
XM_005270287.1:c.822G>A XP_005270344.1:p.Ser274=
XM_005270287.2:c.822G>A XP_005270344.1:p.Ser274=
NM_004281.4:c.822G>A MANE Select NP_004272.2:p.Ser274=
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Search 100 bp 3'