Canonical Allele Identifier: CA378296758
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413483
ClinVar RCV Id: RCV001925971
dbSNP Id: rs1847242044
gnomAD v3: 10-119676722-G-A
gnomAD v4: 10-119676722-G-A
MyVariant Identifiers: chr10:g.121436234G>A (hg19) chr10:g.119676722G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676722G>A , CM000672.2:g.119676722G>A GRCh38
NC_000010.10:g.121436234G>A , CM000672.1:g.121436234G>A GRCh37
NC_000010.9:g.121426224G>A NCBI36
NG_016125.1:g.30353G>A , LRG_742:g.30353G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1168G>A MANE Select ENSP00000358081.4:p.Val390Met
ENST00000369085.7:c.1168G>A ENSP00000358081.3:p.Val390Met
NM_004281.3:c.1168G>A , LRG_742t1:c.1168G>A NP_004272.2:p.Val390Met
XM_005270287.1:c.1165G>A XP_005270344.1:p.Val389Met
XM_005270287.2:c.1165G>A XP_005270344.1:p.Val389Met
NM_004281.4:c.1168G>A MANE Select NP_004272.2:p.Val390Met
Search 100 bp 5'
Search 100 bp 3'