Canonical Allele Identifier: CA378297615
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1511683
ClinVar RCV Id: RCV002020537 RCV002398106
dbSNP Id: rs2134069468
gnomAD v4: 10-119677128-T-C
MyVariant Identifiers: chr10:g.121436640T>C (hg19) chr10:g.119677128T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677128T>C , CM000672.2:g.119677128T>C GRCh38
NC_000010.10:g.121436640T>C , CM000672.1:g.121436640T>C GRCh37
NC_000010.9:g.121426630T>C NCBI36
NG_016125.1:g.30759T>C , LRG_742:g.30759T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1574T>C MANE Select ENSP00000358081.4:p.Met525Thr
ENST00000369085.7:c.1574T>C ENSP00000358081.3:p.Met525Thr
NM_004281.3:c.1574T>C , LRG_742t1:c.1574T>C NP_004272.2:p.Met525Thr
XM_005270287.1:c.1571T>C XP_005270344.1:p.Met524Thr
XM_005270287.2:c.1571T>C XP_005270344.1:p.Met524Thr
NM_004281.4:c.1574T>C MANE Select NP_004272.2:p.Met525Thr
Search 100 bp 5'
Search 100 bp 3'