Canonical Allele Identifier: CA378297457
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1308023
ClinVar RCV Id: RCV001772878
dbSNP Id: rs2134069399
MyVariant Identifiers: chr10:g.121436565A>T (hg19) chr10:g.119677053A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677053A>T , CM000672.2:g.119677053A>T GRCh38
NC_000010.10:g.121436565A>T , CM000672.1:g.121436565A>T GRCh37
NC_000010.9:g.121426555A>T NCBI36
NG_016125.1:g.30684A>T , LRG_742:g.30684A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1499A>T MANE Select ENSP00000358081.4:p.Asp500Val
ENST00000369085.7:c.1499A>T ENSP00000358081.3:p.Asp500Val
NM_004281.3:c.1499A>T , LRG_742t1:c.1499A>T NP_004272.2:p.Asp500Val
XM_005270287.1:c.1496A>T XP_005270344.1:p.Asp499Val
XM_005270287.2:c.1496A>T XP_005270344.1:p.Asp499Val
NM_004281.4:c.1499A>T MANE Select NP_004272.2:p.Asp500Val
Search 100 bp 5'
Search 100 bp 3'