Canonical Allele Identifier: CA261129
Gene: BAG3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 39464
dbSNP Id: rs397514506

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672399C>T , CM000672.2:g.119672399C>T GRCh38
NC_000010.10:g.121431911C>T , CM000672.1:g.121431911C>T GRCh37
NC_000010.9:g.121421901C>T NCBI36
NG_016125.1:g.26030C>T , LRG_742:g.26030C>T

Transcript Alleles

HGVS Amino-acid change
NM_004281.3:c.652C>T , LRG_742t1:c.652C>T NP_004272.2:p.Arg218Trp
XM_005270287.1:c.652C>T XP_005270344.1:p.Arg218Trp
XM_005270287.2:c.652C>T XP_005270344.1:p.Arg218Trp
ENST00000369085.7:c.652C>T ENSP00000358081.3:p.Arg218Trp
ENST00000450186.1:c.478C>T ENSP00000410036.1:p.Arg160Trp