Canonical Allele Identifier: CA471739154
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121431781A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672269A>T , CM000672.2:g.119672269A>T GRCh38
NC_000010.10:g.121431781A>T , CM000672.1:g.121431781A>T GRCh37
NC_000010.9:g.121421771A>T NCBI36
NG_016125.1:g.25900A>T , LRG_742:g.25900A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.522A>T MANE Select ENSP00000358081.4:p.Pro174=
ENST00000369085.7:c.522A>T ENSP00000358081.3:p.Pro174=
ENST00000450186.1:c.348A>T ENSP00000410036.1:p.Pro116=
NM_004281.3:c.522A>T , LRG_742t1:c.522A>T NP_004272.2:p.Pro174=
XM_005270287.1:c.522A>T XP_005270344.1:p.Pro174=
XM_005270287.2:c.522A>T XP_005270344.1:p.Pro174=
NM_004281.4:c.522A>T MANE Select NP_004272.2:p.Pro174=