Canonical Allele Identifier: CA471739189
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121431826T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672314T>A , CM000672.2:g.119672314T>A GRCh38
NC_000010.10:g.121431826T>A , CM000672.1:g.121431826T>A GRCh37
NC_000010.9:g.121421816T>A NCBI36
NG_016125.1:g.25945T>A , LRG_742:g.25945T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.567T>A MANE Select ENSP00000358081.4:p.Pro189=
ENST00000369085.7:c.567T>A ENSP00000358081.3:p.Pro189=
ENST00000450186.1:c.393T>A ENSP00000410036.1:p.Pro131=
NM_004281.3:c.567T>A , LRG_742t1:c.567T>A NP_004272.2:p.Pro189=
XM_005270287.1:c.567T>A XP_005270344.1:p.Pro189=
XM_005270287.2:c.567T>A XP_005270344.1:p.Pro189=
NM_004281.4:c.567T>A MANE Select NP_004272.2:p.Pro189=