Canonical Allele Identifier: CA378294764
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2185740
ClinVar RCV Id: RCV002619821
gnomAD v4: 10-119669941-C-T
MyVariant Identifiers: chr10:g.121429453C>T (hg19) chr10:g.119669941C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669941C>T , CM000672.2:g.119669941C>T GRCh38
NC_000010.10:g.121429453C>T , CM000672.1:g.121429453C>T GRCh37
NC_000010.9:g.121419443C>T NCBI36
NG_016125.1:g.23572C>T , LRG_742:g.23572C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.271C>T MANE Select ENSP00000358081.4:p.Pro91Ser
ENST00000369085.7:c.271C>T ENSP00000358081.3:p.Pro91Ser
ENST00000450186.1:c.97C>T ENSP00000410036.1:p.Pro33Ser
NM_004281.3:c.271C>T , LRG_742t1:c.271C>T NP_004272.2:p.Pro91Ser
XM_005270287.1:c.271C>T XP_005270344.1:p.Pro91Ser
XM_005270287.2:c.271C>T XP_005270344.1:p.Pro91Ser
NM_004281.4:c.271C>T MANE Select NP_004272.2:p.Pro91Ser
Search 100 bp 5'
Search 100 bp 3'