Canonical Allele Identifier: CA378295152
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353582
ClinVar RCV Id: RCV001863485
dbSNP Id: rs572038196
gnomAD v4: 10-119670137-C-A
MyVariant Identifiers: chr10:g.121429649C>A (hg19) chr10:g.119670137C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670137C>A , CM000672.2:g.119670137C>A GRCh38
NC_000010.10:g.121429649C>A , CM000672.1:g.121429649C>A GRCh37
NC_000010.9:g.121419639C>A NCBI36
NG_016125.1:g.23768C>A , LRG_742:g.23768C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.467C>A MANE Select ENSP00000358081.4:p.Ala156Glu
ENST00000369085.7:c.467C>A ENSP00000358081.3:p.Ala156Glu
ENST00000450186.1:c.293C>A ENSP00000410036.1:p.Ala98Glu
NM_004281.3:c.467C>A , LRG_742t1:c.467C>A NP_004272.2:p.Ala156Glu
XM_005270287.1:c.467C>A XP_005270344.1:p.Ala156Glu
XM_005270287.2:c.467C>A XP_005270344.1:p.Ala156Glu
NM_004281.4:c.467C>A MANE Select NP_004272.2:p.Ala156Glu
Search 100 bp 5'
Search 100 bp 3'