Canonical Allele Identifier: CA214221736
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 700725
ClinVar RCV Id: RCV000869024 RCV002352559
dbSNP Id: rs1047671466
gnomAD v3: 10-119672354-C-A
gnomAD v4: 10-119672354-C-A
MyVariant Identifiers: chr10:g.121431866C>A (hg19) chr10:g.119672354C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672354C>A , CM000672.2:g.119672354C>A GRCh38
NC_000010.10:g.121431866C>A , CM000672.1:g.121431866C>A GRCh37
NC_000010.9:g.121421856C>A NCBI36
NG_016125.1:g.25985C>A , LRG_742:g.25985C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.607C>A MANE Select ENSP00000358081.4:p.Arg203=
ENST00000369085.7:c.607C>A ENSP00000358081.3:p.Arg203=
ENST00000450186.1:c.433C>A ENSP00000410036.1:p.Arg145=
NM_004281.3:c.607C>A , LRG_742t1:c.607C>A NP_004272.2:p.Arg203=
XM_005270287.1:c.607C>A XP_005270344.1:p.Arg203=
XM_005270287.2:c.607C>A XP_005270344.1:p.Arg203=
NM_004281.4:c.607C>A MANE Select NP_004272.2:p.Arg203=
Search 100 bp 5'
Search 100 bp 3'