Canonical Allele Identifier: CA378294193
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 949224
ClinVar RCV Id: RCV001220639 RCV003163698
dbSNP Id: rs1846844070
gnomAD v4: 10-119651783-G-A
MyVariant Identifiers: chr10:g.121411295G>A (hg19) chr10:g.119651783G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651783G>A , CM000672.2:g.119651783G>A GRCh38
NC_000010.10:g.121411295G>A , CM000672.1:g.121411295G>A GRCh37
NC_000010.9:g.121401285G>A NCBI36
NG_016125.1:g.5414G>A , LRG_742:g.5414G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.108G>A MANE Select ENSP00000358081.4:p.Trp36Ter
ENST00000369085.7:c.108G>A ENSP00000358081.3:p.Trp36Ter
NM_004281.3:c.108G>A , LRG_742t1:c.108G>A NP_004272.2:p.Trp36Ter
XM_005270287.1:c.108G>A XP_005270344.1:p.Trp36Ter
XM_005270287.2:c.108G>A XP_005270344.1:p.Trp36Ter
NM_004281.4:c.108G>A MANE Select NP_004272.2:p.Trp36Ter
Search 100 bp 5'
Search 100 bp 3'