Canonical Allele Identifier: CA378294183
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1388942
ClinVar RCV Id: RCV001886920
dbSNP Id: rs200072558
gnomAD v4: 10-119651778-G-T
MyVariant Identifiers: chr10:g.121411290G>T (hg19) chr10:g.119651778G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.103G>T MANE Select ENSP00000358081.4:p.Gly35Cys
ENST00000369085.7:c.103G>T ENSP00000358081.3:p.Gly35Cys
NM_004281.3:c.103G>T , LRG_742t1:c.103G>T NP_004272.2:p.Gly35Cys
XM_005270287.1:c.103G>T XP_005270344.1:p.Gly35Cys
XM_005270287.2:c.103G>T XP_005270344.1:p.Gly35Cys
NM_004281.4:c.103G>T MANE Select NP_004272.2:p.Gly35Cys
Search 100 bp 5'
Search 100 bp 3'