Canonical Allele Identifier: CA10635036
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 298961
ClinVar RCV Id: RCV000402177 RCV000306231 RCV002522142 RCV002392833
dbSNP Id: rs147277075
gnomAD v2: 10-121436569-C-T
gnomAD v3: 10-119677057-C-T
gnomAD v4: 10-119677057-C-T
MyVariant Identifiers: chr10:g.121436569C>T (hg19) chr10:g.119677057C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677057C>T , CM000672.2:g.119677057C>T GRCh38
NC_000010.10:g.121436569C>T , CM000672.1:g.121436569C>T GRCh37
NC_000010.9:g.121426559C>T NCBI36
NG_016125.1:g.30688C>T , LRG_742:g.30688C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1503C>T MANE Select ENSP00000358081.4:p.Val501=
ENST00000369085.7:c.1503C>T ENSP00000358081.3:p.Val501=
NM_004281.3:c.1503C>T , LRG_742t1:c.1503C>T NP_004272.2:p.Val501=
XM_005270287.1:c.1500C>T XP_005270344.1:p.Val500=
XM_005270287.2:c.1500C>T XP_005270344.1:p.Val500=
NM_004281.4:c.1503C>T MANE Select NP_004272.2:p.Val501=
Search 100 bp 5'
Search 100 bp 3'