Canonical Allele Identifier: CA214207826
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 877092
ClinVar RCV Id: RCV001102545 RCV001104463
dbSNP Id: rs913687992
gnomAD v2: 10-121411102-G-A
gnomAD v3: 10-119651590-G-A
gnomAD v4: 10-119651590-G-A
MyVariant Identifiers: chr10:g.121411102G>A (hg19) chr10:g.119651590G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651590G>A , CM000672.2:g.119651590G>A GRCh38
NC_000010.10:g.121411102G>A , CM000672.1:g.121411102G>A GRCh37
NC_000010.9:g.121401092G>A NCBI36
NG_016125.1:g.5221G>A , LRG_742:g.5221G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.-86G>A MANE Select ENSP00000358081.4:n.-86G>A
ENST00000369085.7:c.-86G>A ENSP00000358081.3:n.-86G>A
NM_004281.3:c.-86G>A , LRG_742t1:c.-86G>A NP_004272.2:n.-86G>A
XM_005270287.1:c.-86G>A XP_005270344.1:n.-86G>A
XM_005270287.2:c.-86G>A XP_005270344.1:n.-86G>A
NM_004281.4:c.-86G>A MANE Select NP_004272.2:n.-86G>A
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