Canonical Allele Identifier: CA282458
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 44777
ClinVar RCV Id: RCV000037886 RCV000243961 RCV000399004 RCV000576644 RCV000590573 RCV001509888
dbSNP Id: rs196295
ExAC: 10:121436362 A / G
gnomAD v2: 10-121436362-A-G
gnomAD v3: 10-119676850-A-G
gnomAD v4: 10-119676850-A-G
MyVariant Identifiers: chr10:g.121436362A>G (hg19) chr10:g.119676850A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676850A>G , CM000672.2:g.119676850A>G GRCh38
NC_000010.10:g.121436362A>G , CM000672.1:g.121436362A>G GRCh37
NC_000010.9:g.121426352A>G NCBI36
NG_016125.1:g.30481A>G , LRG_742:g.30481A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1296A>G MANE Select ENSP00000358081.4:p.Val432=
ENST00000369085.7:c.1296A>G ENSP00000358081.3:p.Val432=
NM_004281.3:c.1296A>G , LRG_742t1:c.1296A>G NP_004272.2:p.Val432=
XM_005270287.1:c.1293A>G XP_005270344.1:p.Val431=
XM_005270287.2:c.1293A>G XP_005270344.1:p.Val431=
NM_004281.4:c.1296A>G MANE Select NP_004272.2:p.Val432=
Search 100 bp 5'
Search 100 bp 3'