Canonical Allele Identifier: CA5716217
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462897
ClinVar RCV Id: RCV001954378
dbSNP Id: rs200072558
ExAC: 10:121411290 G / A
gnomAD v2: 10-121411290-G-A
gnomAD v3: 10-119651778-G-A
gnomAD v4: 10-119651778-G-A
MyVariant Identifiers: chr10:g.121411290G>A (hg19) chr10:g.119651778G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651778G>A , CM000672.2:g.119651778G>A GRCh38
NC_000010.10:g.121411290G>A , CM000672.1:g.121411290G>A GRCh37
NC_000010.9:g.121401280G>A NCBI36
NG_016125.1:g.5409G>A , LRG_742:g.5409G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.103G>A MANE Select ENSP00000358081.4:p.Gly35Ser
ENST00000369085.7:c.103G>A ENSP00000358081.3:p.Gly35Ser
NM_004281.3:c.103G>A , LRG_742t1:c.103G>A NP_004272.2:p.Gly35Ser
XM_005270287.1:c.103G>A XP_005270344.1:p.Gly35Ser
XM_005270287.2:c.103G>A XP_005270344.1:p.Gly35Ser
NM_004281.4:c.103G>A MANE Select NP_004272.2:p.Gly35Ser
Search 100 bp 5'
Search 100 bp 3'