Canonical Allele Identifier: CA135019
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 44781
ClinVar RCV Id: RCV000037890 RCV000231536 RCV000395368 RCV000341377 RCV001528415
dbSNP Id: rs143752613
ExAC: 10:121429413 G / A
gnomAD v2: 10-121429413-G-A
gnomAD v3: 10-119669901-G-A
gnomAD v4: 10-119669901-G-A
MyVariant Identifiers: chr10:g.121429413G>A (hg19) chr10:g.119669901G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669901G>A , CM000672.2:g.119669901G>A GRCh38
NC_000010.10:g.121429413G>A , CM000672.1:g.121429413G>A GRCh37
NC_000010.9:g.121419403G>A NCBI36
NG_016125.1:g.23532G>A , LRG_742:g.23532G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.231G>A MANE Select ENSP00000358081.4:p.Pro77=
ENST00000369085.7:c.231G>A ENSP00000358081.3:p.Pro77=
ENST00000450186.1:c.57G>A ENSP00000410036.1:p.Pro19=
NM_004281.3:c.231G>A , LRG_742t1:c.231G>A NP_004272.2:p.Pro77=
XM_005270287.1:c.231G>A XP_005270344.1:p.Pro77=
XM_005270287.2:c.231G>A XP_005270344.1:p.Pro77=
NM_004281.4:c.231G>A MANE Select NP_004272.2:p.Pro77=
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