Canonical Allele Identifier: CA378295909
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011211
dbSNP Id: rs1847167969

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672591A>G , CM000672.2:g.119672591A>G GRCh38
NC_000010.10:g.121432103A>G , CM000672.1:g.121432103A>G GRCh37
NC_000010.9:g.121422093A>G NCBI36
NG_016125.1:g.26222A>G , LRG_742:g.26222A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.844A>G MANE Select ENSP00000358081.4:p.Arg282Gly
ENST00000369085.7:c.844A>G ENSP00000358081.3:p.Arg282Gly
ENST00000450186.1:c.670A>G ENSP00000410036.1:p.Arg224Gly
NM_004281.3:c.844A>G , LRG_742t1:c.844A>G NP_004272.2:p.Arg282Gly
XM_005270287.1:c.844A>G XP_005270344.1:p.Arg282Gly
XM_005270287.2:c.844A>G XP_005270344.1:p.Arg282Gly
NM_004281.4:c.844A>G MANE Select NP_004272.2:p.Arg282Gly