Canonical Allele Identifier: CA378297608
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1432923
ClinVar RCV Id: RCV002397948 RCV001982135
dbSNP Id: rs764925485
gnomAD v2: 10-121436636-A-T
gnomAD v4: 10-119677124-A-T
MyVariant Identifiers: chr10:g.121436636A>T (hg19) chr10:g.119677124A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677124A>T , CM000672.2:g.119677124A>T GRCh38
NC_000010.10:g.121436636A>T , CM000672.1:g.121436636A>T GRCh37
NC_000010.9:g.121426626A>T NCBI36
NG_016125.1:g.30755A>T , LRG_742:g.30755A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1570A>T MANE Select ENSP00000358081.4:p.Ile524Phe
ENST00000369085.7:c.1570A>T ENSP00000358081.3:p.Ile524Phe
NM_004281.3:c.1570A>T , LRG_742t1:c.1570A>T NP_004272.2:p.Ile524Phe
XM_005270287.1:c.1567A>T XP_005270344.1:p.Ile523Phe
XM_005270287.2:c.1567A>T XP_005270344.1:p.Ile523Phe
NM_004281.4:c.1570A>T MANE Select NP_004272.2:p.Ile524Phe
Search 100 bp 5'
Search 100 bp 3'