Canonical Allele Identifier: CA378297347
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1464430
ClinVar RCV Id: RCV001975453
dbSNP Id: rs2134069371

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677007A>G , CM000672.2:g.119677007A>G GRCh38
NC_000010.10:g.121436519A>G , CM000672.1:g.121436519A>G GRCh37
NC_000010.9:g.121426509A>G NCBI36
NG_016125.1:g.30638A>G , LRG_742:g.30638A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1453A>G MANE Select ENSP00000358081.4:p.Arg485Gly
ENST00000369085.7:c.1453A>G ENSP00000358081.3:p.Arg485Gly
NM_004281.3:c.1453A>G , LRG_742t1:c.1453A>G NP_004272.2:p.Arg485Gly
XM_005270287.1:c.1450A>G XP_005270344.1:p.Arg484Gly
XM_005270287.2:c.1450A>G XP_005270344.1:p.Arg484Gly
NM_004281.4:c.1453A>G MANE Select NP_004272.2:p.Arg485Gly