Canonical Allele Identifier: CA282467
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 44783
dbSNP Id: rs2234962

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670121T>C , CM000672.2:g.119670121T>C GRCh38
NC_000010.10:g.121429633T>C , CM000672.1:g.121429633T>C GRCh37
NC_000010.9:g.121419623T>C NCBI36
NG_016125.1:g.23752T>C , LRG_742:g.23752T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.451T>C MANE Select ENSP00000358081.4:p.Cys151Arg
ENST00000369085.7:c.451T>C ENSP00000358081.3:p.Cys151Arg
ENST00000450186.1:c.277T>C ENSP00000410036.1:p.Cys93Arg
NM_004281.3:c.451T>C , LRG_742t1:c.451T>C NP_004272.2:p.Cys151Arg
XM_005270287.1:c.451T>C XP_005270344.1:p.Cys151Arg
XM_005270287.2:c.451T>C XP_005270344.1:p.Cys151Arg
NM_004281.4:c.451T>C MANE Select NP_004272.2:p.Cys151Arg