Canonical Allele Identifier: CA471740217
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1147302
ClinVar RCV Id: RCV001486801
dbSNP Id: rs776700820
gnomAD v4: 10-119672569-G-T
MyVariant Identifiers: chr10:g.121432081G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672569G>T , CM000672.2:g.119672569G>T GRCh38
NC_000010.10:g.121432081G>T , CM000672.1:g.121432081G>T GRCh37
NC_000010.9:g.121422071G>T NCBI36
NG_016125.1:g.26200G>T , LRG_742:g.26200G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.822G>T MANE Select ENSP00000358081.4:p.Ser274=
ENST00000369085.7:c.822G>T ENSP00000358081.3:p.Ser274=
ENST00000450186.1:c.648G>T ENSP00000410036.1:p.Ser216=
NM_004281.3:c.822G>T , LRG_742t1:c.822G>T NP_004272.2:p.Ser274=
XM_005270287.1:c.822G>T XP_005270344.1:p.Ser274=
XM_005270287.2:c.822G>T XP_005270344.1:p.Ser274=
NM_004281.4:c.822G>T MANE Select NP_004272.2:p.Ser274=
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