Canonical Allele Identifier: CA5716278
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2945378
ClinVar RCV Id: RCV003801032
dbSNP Id: rs755525021
ExAC: 10:121429451 G / A
gnomAD v2: 10-121429451-G-A
gnomAD v4: 10-119669939-G-A
MyVariant Identifiers: chr10:g.121429451G>A (hg19) chr10:g.119669939G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669939G>A , CM000672.2:g.119669939G>A GRCh38
NC_000010.10:g.121429451G>A , CM000672.1:g.121429451G>A GRCh37
NC_000010.9:g.121419441G>A NCBI36
NG_016125.1:g.23570G>A , LRG_742:g.23570G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.269G>A MANE Select ENSP00000358081.4:p.Arg90Gln
ENST00000369085.7:c.269G>A ENSP00000358081.3:p.Arg90Gln
ENST00000450186.1:c.95G>A ENSP00000410036.1:p.Arg32Gln
NM_004281.3:c.269G>A , LRG_742t1:c.269G>A NP_004272.2:p.Arg90Gln
XM_005270287.1:c.269G>A XP_005270344.1:p.Arg90Gln
XM_005270287.2:c.269G>A XP_005270344.1:p.Arg90Gln
NM_004281.4:c.269G>A MANE Select NP_004272.2:p.Arg90Gln
Search 100 bp 5'
Search 100 bp 3'