Canonical Allele Identifier: CA596322942
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1194914335
gnomAD v2: 10-121411055-T-A
gnomAD v3: 10-119651543-T-A
gnomAD v4: 10-119651543-T-A
MyVariant Identifiers: chr10:g.121411055T>A (hg19) chr10:g.119651543T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651543T>A , CM000672.2:g.119651543T>A GRCh38
NC_000010.10:g.121411055T>A , CM000672.1:g.121411055T>A GRCh37
NC_000010.9:g.121401045T>A NCBI36
NG_016125.1:g.5174T>A , LRG_742:g.5174T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.-133T>A MANE Select ENSP00000358081.4:n.-133T>A
ENST00000369085.7:c.-133T>A ENSP00000358081.3:n.-133T>A
NM_004281.3:c.-133T>A , LRG_742t1:c.-133T>A NP_004272.2:n.-133T>A
XM_005270287.1:c.-133T>A XP_005270344.1:n.-133T>A
XM_005270287.2:c.-133T>A XP_005270344.1:n.-133T>A
NM_004281.4:c.-133T>A MANE Select NP_004272.2:n.-133T>A
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