Canonical Allele Identifier: CA214221835
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1024582658

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672436A>G , CM000672.2:g.119672436A>G GRCh38
NC_000010.10:g.121431948A>G , CM000672.1:g.121431948A>G GRCh37
NC_000010.9:g.121421938A>G NCBI36
NG_016125.1:g.26067A>G , LRG_742:g.26067A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.689A>G MANE Select ENSP00000358081.4:p.Lys230Arg
ENST00000369085.7:c.689A>G ENSP00000358081.3:p.Lys230Arg
ENST00000450186.1:c.515A>G ENSP00000410036.1:p.Lys172Arg
NM_004281.3:c.689A>G , LRG_742t1:c.689A>G NP_004272.2:p.Lys230Arg
XM_005270287.1:c.689A>G XP_005270344.1:p.Lys230Arg
XM_005270287.2:c.689A>G XP_005270344.1:p.Lys230Arg
NM_004281.4:c.689A>G MANE Select NP_004272.2:p.Lys230Arg