Canonical Allele Identifier: CA5716290
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 794214
ClinVar RCV Id: RCV001475607 RCV003169496
dbSNP Id: rs750075933
ExAC: 10:121429500 G / T
gnomAD v2: 10-121429500-G-T
gnomAD v3: 10-119669988-G-T
gnomAD v4: 10-119669988-G-T
MyVariant Identifiers: chr10:g.121429500G>T (hg19) chr10:g.119669988G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669988G>T , CM000672.2:g.119669988G>T GRCh38
NC_000010.10:g.121429500G>T , CM000672.1:g.121429500G>T GRCh37
NC_000010.9:g.121419490G>T NCBI36
NG_016125.1:g.23619G>T , LRG_742:g.23619G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.318G>T MANE Select ENSP00000358081.4:p.Arg106=
ENST00000369085.7:c.318G>T ENSP00000358081.3:p.Arg106=
ENST00000450186.1:c.144G>T ENSP00000410036.1:p.Arg48=
NM_004281.3:c.318G>T , LRG_742t1:c.318G>T NP_004272.2:p.Arg106=
XM_005270287.1:c.318G>T XP_005270344.1:p.Arg106=
XM_005270287.2:c.318G>T XP_005270344.1:p.Arg106=
NM_004281.4:c.318G>T MANE Select NP_004272.2:p.Arg106=
Search 100 bp 5'
Search 100 bp 3'