Canonical Allele Identifier: CA471634528
Gene: BAG3 HGNC NCBI

Linked Data

gnomAD v4: 10-119670039-A-G
MyVariant Identifiers: chr10:g.121429551A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670039A>G , CM000672.2:g.119670039A>G GRCh38
NC_000010.10:g.121429551A>G , CM000672.1:g.121429551A>G GRCh37
NC_000010.9:g.121419541A>G NCBI36
NG_016125.1:g.23670A>G , LRG_742:g.23670A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.369A>G MANE Select ENSP00000358081.4:p.Arg123=
ENST00000369085.7:c.369A>G ENSP00000358081.3:p.Arg123=
ENST00000450186.1:c.195A>G ENSP00000410036.1:p.Arg65=
NM_004281.3:c.369A>G , LRG_742t1:c.369A>G NP_004272.2:p.Arg123=
XM_005270287.1:c.369A>G XP_005270344.1:p.Arg123=
XM_005270287.2:c.369A>G XP_005270344.1:p.Arg123=
NM_004281.4:c.369A>G MANE Select NP_004272.2:p.Arg123=
Search 100 bp 5'
Search 100 bp 3'