Canonical Allele Identifier: CA378295483
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 879636
ClinVar RCV Id: RCV001107315 RCV001107314 RCV002556099
dbSNP Id: rs1311591078
gnomAD v2: 10-121431896-G-A
gnomAD v4: 10-119672384-G-A
MyVariant Identifiers: chr10:g.121431896G>A (hg19) chr10:g.119672384G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672384G>A , CM000672.2:g.119672384G>A GRCh38
NC_000010.10:g.121431896G>A , CM000672.1:g.121431896G>A GRCh37
NC_000010.9:g.121421886G>A NCBI36
NG_016125.1:g.26015G>A , LRG_742:g.26015G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.637G>A MANE Select ENSP00000358081.4:p.Glu213Lys
ENST00000369085.7:c.637G>A ENSP00000358081.3:p.Glu213Lys
ENST00000450186.1:c.463G>A ENSP00000410036.1:p.Glu155Lys
NM_004281.3:c.637G>A , LRG_742t1:c.637G>A NP_004272.2:p.Glu213Lys
XM_005270287.1:c.637G>A XP_005270344.1:p.Glu213Lys
XM_005270287.2:c.637G>A XP_005270344.1:p.Glu213Lys
NM_004281.4:c.637G>A MANE Select NP_004272.2:p.Glu213Lys
Search 100 bp 5'
Search 100 bp 3'