Canonical Allele Identifier: CA5716398
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349860
ClinVar RCV Id: RCV002039320
dbSNP Id: rs371731106
ExAC: 10:121431963 C / T
gnomAD v2: 10-121431963-C-T
gnomAD v3: 10-119672451-C-T
gnomAD v4: 10-119672451-C-T
MyVariant Identifiers: chr10:g.121431963C>T (hg19) chr10:g.119672451C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672451C>T , CM000672.2:g.119672451C>T GRCh38
NC_000010.10:g.121431963C>T , CM000672.1:g.121431963C>T GRCh37
NC_000010.9:g.121421953C>T NCBI36
NG_016125.1:g.26082C>T , LRG_742:g.26082C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.704C>T MANE Select ENSP00000358081.4:p.Ala235Val
ENST00000369085.7:c.704C>T ENSP00000358081.3:p.Ala235Val
ENST00000450186.1:c.530C>T ENSP00000410036.1:p.Ala177Val
NM_004281.3:c.704C>T , LRG_742t1:c.704C>T NP_004272.2:p.Ala235Val
XM_005270287.1:c.704C>T XP_005270344.1:p.Ala235Val
XM_005270287.2:c.704C>T XP_005270344.1:p.Ala235Val
NM_004281.4:c.704C>T MANE Select NP_004272.2:p.Ala235Val
Search 100 bp 5'
Search 100 bp 3'