Canonical Allele Identifier: CA5716264
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3223772
ClinVar RCV Id: RCV004516536
dbSNP Id: rs572036022
ExAC: 10:121429382 A / C
gnomAD v2: 10-121429382-A-C
gnomAD v3: 10-119669870-A-C
gnomAD v4: 10-119669870-A-C
MyVariant Identifiers: chr10:g.121429382A>C (hg19) chr10:g.119669870A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669870A>C , CM000672.2:g.119669870A>C GRCh38
NC_000010.10:g.121429382A>C , CM000672.1:g.121429382A>C GRCh37
NC_000010.9:g.121419372A>C NCBI36
NG_016125.1:g.23501A>C , LRG_742:g.23501A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.200A>C MANE Select ENSP00000358081.4:p.Asn67Thr
ENST00000369085.7:c.200A>C ENSP00000358081.3:p.Asn67Thr
ENST00000450186.1:c.26A>C ENSP00000410036.1:p.Asn9Thr
NM_004281.3:c.200A>C , LRG_742t1:c.200A>C NP_004272.2:p.Asn67Thr
XM_005270287.1:c.200A>C XP_005270344.1:p.Asn67Thr
XM_005270287.2:c.200A>C XP_005270344.1:p.Asn67Thr
NM_004281.4:c.200A>C MANE Select NP_004272.2:p.Asn67Thr
Search 100 bp 5'
Search 100 bp 3'