Canonical Allele Identifier: CA471634057
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121411289C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651777C>A , CM000672.2:g.119651777C>A GRCh38
NC_000010.10:g.121411289C>A , CM000672.1:g.121411289C>A GRCh37
NC_000010.9:g.121401279C>A NCBI36
NG_016125.1:g.5408C>A , LRG_742:g.5408C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.102C>A MANE Select ENSP00000358081.4:p.Thr34=
ENST00000369085.7:c.102C>A ENSP00000358081.3:p.Thr34=
NM_004281.3:c.102C>A , LRG_742t1:c.102C>A NP_004272.2:p.Thr34=
XM_005270287.1:c.102C>A XP_005270344.1:p.Thr34=
XM_005270287.2:c.102C>A XP_005270344.1:p.Thr34=
NM_004281.4:c.102C>A MANE Select NP_004272.2:p.Thr34=