Canonical Allele Identifier: CA5716573
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165166
ClinVar RCV Id: RCV003084226 RCV004073122
dbSNP Id: rs759058143
ExAC: 10:121436633 G / A
gnomAD v2: 10-121436633-G-A
gnomAD v3: 10-119677121-G-A
gnomAD v4: 10-119677121-G-A
MyVariant Identifiers: chr10:g.121436633G>A (hg19) chr10:g.119677121G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677121G>A , CM000672.2:g.119677121G>A GRCh38
NC_000010.10:g.121436633G>A , CM000672.1:g.121436633G>A GRCh37
NC_000010.9:g.121426623G>A NCBI36
NG_016125.1:g.30752G>A , LRG_742:g.30752G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1567G>A MANE Select ENSP00000358081.4:p.Ala523Thr
ENST00000369085.7:c.1567G>A ENSP00000358081.3:p.Ala523Thr
NM_004281.3:c.1567G>A , LRG_742t1:c.1567G>A NP_004272.2:p.Ala523Thr
XM_005270287.1:c.1564G>A XP_005270344.1:p.Ala522Thr
XM_005270287.2:c.1564G>A XP_005270344.1:p.Ala522Thr
NM_004281.4:c.1567G>A MANE Select NP_004272.2:p.Ala523Thr
Search 100 bp 5'
Search 100 bp 3'