Canonical Allele Identifier: CA5716400
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1134961
ClinVar RCV Id: RCV001470058 RCV003326577
dbSNP Id: rs377183466
ExAC: 10:121431973 G / A
gnomAD v2: 10-121431973-G-A
gnomAD v4: 10-119672461-G-A
MyVariant Identifiers: chr10:g.121431973G>A (hg19) chr10:g.119672461G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672461G>A , CM000672.2:g.119672461G>A GRCh38
NC_000010.10:g.121431973G>A , CM000672.1:g.121431973G>A GRCh37
NC_000010.9:g.121421963G>A NCBI36
NG_016125.1:g.26092G>A , LRG_742:g.26092G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.714G>A MANE Select ENSP00000358081.4:p.Gly238=
ENST00000369085.7:c.714G>A ENSP00000358081.3:p.Gly238=
ENST00000450186.1:c.540G>A ENSP00000410036.1:p.Gly180=
NM_004281.3:c.714G>A , LRG_742t1:c.714G>A NP_004272.2:p.Gly238=
XM_005270287.1:c.714G>A XP_005270344.1:p.Gly238=
XM_005270287.2:c.714G>A XP_005270344.1:p.Gly238=
NM_004281.4:c.714G>A MANE Select NP_004272.2:p.Gly238=
Search 100 bp 5'
Search 100 bp 3'