Canonical Allele Identifier: CA378295613
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 571982
ClinVar RCV Id: RCV000693263 RCV002360753 RCV001568137
dbSNP Id: rs1415830597
gnomAD v3: 10-119672445-A-G
gnomAD v4: 10-119672445-A-G
MyVariant Identifiers: chr10:g.121431957A>G (hg19) chr10:g.119672445A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672445A>G , CM000672.2:g.119672445A>G GRCh38
NC_000010.10:g.121431957A>G , CM000672.1:g.121431957A>G GRCh37
NC_000010.9:g.121421947A>G NCBI36
NG_016125.1:g.26076A>G , LRG_742:g.26076A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.698A>G MANE Select ENSP00000358081.4:p.Tyr233Cys
ENST00000369085.7:c.698A>G ENSP00000358081.3:p.Tyr233Cys
ENST00000450186.1:c.524A>G ENSP00000410036.1:p.Tyr175Cys
NM_004281.3:c.698A>G , LRG_742t1:c.698A>G NP_004272.2:p.Tyr233Cys
XM_005270287.1:c.698A>G XP_005270344.1:p.Tyr233Cys
XM_005270287.2:c.698A>G XP_005270344.1:p.Tyr233Cys
NM_004281.4:c.698A>G MANE Select NP_004272.2:p.Tyr233Cys
Search 100 bp 5'
Search 100 bp 3'