Canonical Allele Identifier: CA378296763
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2575034
ClinVar RCV Id: RCV003319931 RCV003396999
MyVariant Identifiers: chr10:g.121436235T>G (hg19) chr10:g.119676723T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676723T>G , CM000672.2:g.119676723T>G GRCh38
NC_000010.10:g.121436235T>G , CM000672.1:g.121436235T>G GRCh37
NC_000010.9:g.121426225T>G NCBI36
NG_016125.1:g.30354T>G , LRG_742:g.30354T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1169T>G MANE Select ENSP00000358081.4:p.Val390Gly
ENST00000369085.7:c.1169T>G ENSP00000358081.3:p.Val390Gly
NM_004281.3:c.1169T>G , LRG_742t1:c.1169T>G NP_004272.2:p.Val390Gly
XM_005270287.1:c.1166T>G XP_005270344.1:p.Val389Gly
XM_005270287.2:c.1166T>G XP_005270344.1:p.Val389Gly
NM_004281.4:c.1169T>G MANE Select NP_004272.2:p.Val390Gly
Search 100 bp 5'
Search 100 bp 3'