Canonical Allele Identifier: CA5716307
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1155267
ClinVar RCV Id: RCV001497509 RCV002359116
dbSNP Id: rs753235577
ExAC: 10:121429560 G / A
gnomAD v2: 10-121429560-G-A
gnomAD v3: 10-119670048-G-A
gnomAD v4: 10-119670048-G-A
COSMIC: COSM4012088
MyVariant Identifiers: chr10:g.121429560G>A (hg19) chr10:g.119670048G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670048G>A , CM000672.2:g.119670048G>A GRCh38
NC_000010.10:g.121429560G>A , CM000672.1:g.121429560G>A GRCh37
NC_000010.9:g.121419550G>A NCBI36
NG_016125.1:g.23679G>A , LRG_742:g.23679G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.378G>A MANE Select ENSP00000358081.4:p.Ala126=
ENST00000369085.7:c.378G>A ENSP00000358081.3:p.Ala126=
ENST00000450186.1:c.204G>A ENSP00000410036.1:p.Ala68=
NM_004281.3:c.378G>A , LRG_742t1:c.378G>A NP_004272.2:p.Ala126=
XM_005270287.1:c.378G>A XP_005270344.1:p.Ala126=
XM_005270287.2:c.378G>A XP_005270344.1:p.Ala126=
NM_004281.4:c.378G>A MANE Select NP_004272.2:p.Ala126=
Search 100 bp 5'
Search 100 bp 3'