Canonical Allele Identifier: CA378295517
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2505318
ClinVar RCV Id: RCV003319251
dbSNP Id: rs201638005
gnomAD v4: 10-119672400-G-T
MyVariant Identifiers: chr10:g.121431912G>T (hg19) chr10:g.119672400G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672400G>T , CM000672.2:g.119672400G>T GRCh38
NC_000010.10:g.121431912G>T , CM000672.1:g.121431912G>T GRCh37
NC_000010.9:g.121421902G>T NCBI36
NG_016125.1:g.26031G>T , LRG_742:g.26031G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.653G>T MANE Select ENSP00000358081.4:p.Arg218Leu
ENST00000369085.7:c.653G>T ENSP00000358081.3:p.Arg218Leu
ENST00000450186.1:c.479G>T ENSP00000410036.1:p.Arg160Leu
NM_004281.3:c.653G>T , LRG_742t1:c.653G>T NP_004272.2:p.Arg218Leu
XM_005270287.1:c.653G>T XP_005270344.1:p.Arg218Leu
XM_005270287.2:c.653G>T XP_005270344.1:p.Arg218Leu
NM_004281.4:c.653G>T MANE Select NP_004272.2:p.Arg218Leu
Search 100 bp 5'
Search 100 bp 3'