Canonical Allele Identifier: CA5716427
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 383009
ClinVar RCV Id: RCV000618259 RCV001703759 RCV002062562
dbSNP Id: rs140737221
ExAC: 10:121432129 C / A
gnomAD v2: 10-121432129-C-A
gnomAD v4: 10-119672617-C-A
MyVariant Identifiers: chr10:g.121432129C>A (hg19) chr10:g.119672617C>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.870C>A MANE Select ENSP00000358081.4:p.Pro290=
ENST00000369085.7:c.870C>A ENSP00000358081.3:p.Pro290=
ENST00000450186.1:c.696C>A ENSP00000410036.1:p.Pro232=
NM_004281.3:c.870C>A , LRG_742t1:c.870C>A NP_004272.2:p.Pro290=
XM_005270287.1:c.870C>A XP_005270344.1:p.Pro290=
XM_005270287.2:c.870C>A XP_005270344.1:p.Pro290=
NM_004281.4:c.870C>A MANE Select NP_004272.2:p.Pro290=
Search 100 bp 5'
Search 100 bp 3'