Canonical Allele Identifier: CA5716279
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs371026669

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669944G>C , CM000672.2:g.119669944G>C GRCh38
NC_000010.10:g.121429456G>C , CM000672.1:g.121429456G>C GRCh37
NC_000010.9:g.121419446G>C NCBI36
NG_016125.1:g.23575G>C , LRG_742:g.23575G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.274G>C MANE Select ENSP00000358081.4:p.Gly92Arg
ENST00000369085.7:c.274G>C ENSP00000358081.3:p.Gly92Arg
ENST00000450186.1:c.100G>C ENSP00000410036.1:p.Gly34Arg
NM_004281.3:c.274G>C , LRG_742t1:c.274G>C NP_004272.2:p.Gly92Arg
XM_005270287.1:c.274G>C XP_005270344.1:p.Gly92Arg
XM_005270287.2:c.274G>C XP_005270344.1:p.Gly92Arg
NM_004281.4:c.274G>C MANE Select NP_004272.2:p.Gly92Arg