Canonical Allele Identifier: CA5716502
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2155450
ClinVar RCV Id: RCV003090671
dbSNP Id: rs777587890
ExAC: 10:121436233 T / G
gnomAD v2: 10-121436233-T-G
gnomAD v4: 10-119676721-T-G
MyVariant Identifiers: chr10:g.121436233T>G (hg19) chr10:g.119676721T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676721T>G , CM000672.2:g.119676721T>G GRCh38
NC_000010.10:g.121436233T>G , CM000672.1:g.121436233T>G GRCh37
NC_000010.9:g.121426223T>G NCBI36
NG_016125.1:g.30352T>G , LRG_742:g.30352T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1167T>G MANE Select ENSP00000358081.4:p.Ser389Arg
ENST00000369085.7:c.1167T>G ENSP00000358081.3:p.Ser389Arg
NM_004281.3:c.1167T>G , LRG_742t1:c.1167T>G NP_004272.2:p.Ser389Arg
XM_005270287.1:c.1164T>G XP_005270344.1:p.Ser388Arg
XM_005270287.2:c.1164T>G XP_005270344.1:p.Ser388Arg
NM_004281.4:c.1167T>G MANE Select NP_004272.2:p.Ser389Arg
Search 100 bp 5'
Search 100 bp 3'