Canonical Allele Identifier: CA378296038
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1505893
ClinVar RCV Id: RCV001999633
dbSNP Id: rs748451757

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672622C>G , CM000672.2:g.119672622C>G GRCh38
NC_000010.10:g.121432134C>G , CM000672.1:g.121432134C>G GRCh37
NC_000010.9:g.121422124C>G NCBI36
NG_016125.1:g.26253C>G , LRG_742:g.26253C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.875C>G MANE Select ENSP00000358081.4:p.Pro292Arg
ENST00000369085.7:c.875C>G ENSP00000358081.3:p.Pro292Arg
ENST00000450186.1:c.701C>G ENSP00000410036.1:p.Pro234Arg
NM_004281.3:c.875C>G , LRG_742t1:c.875C>G NP_004272.2:p.Pro292Arg
XM_005270287.1:c.875C>G XP_005270344.1:p.Pro292Arg
XM_005270287.2:c.875C>G XP_005270344.1:p.Pro292Arg
NM_004281.4:c.875C>G MANE Select NP_004272.2:p.Pro292Arg