Canonical Allele Identifier: CA10576779
Gene: BAG3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 228322
dbSNP Id: rs869248137

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676479C>T , CM000672.2:g.119676479C>T GRCh38
NC_000010.10:g.121435991C>T , CM000672.1:g.121435991C>T GRCh37
NC_000010.9:g.121425981C>T NCBI36
NG_016125.1:g.30110C>T , LRG_742:g.30110C>T

Transcript Alleles

HGVS Amino-acid change
NM_004281.3:c.925C>T , LRG_742t1:c.925C>T NP_004272.2:p.Arg309Ter
XM_005270287.1:c.922C>T XP_005270344.1:p.Arg308Ter
XM_005270287.2:c.922C>T XP_005270344.1:p.Arg308Ter
ENST00000369085.7:c.925C>T ENSP00000358081.3:p.Arg309Ter
ENST00000450186.1:c.748C>T ENSP00000410036.1:p.Arg250Ter