Canonical Allele Identifier: CA5716501
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2439469
ClinVar RCV Id: RCV003143738 RCV003778828
dbSNP Id: rs752618673
ExAC: 10:121436231 A / G
gnomAD v2: 10-121436231-A-G
gnomAD v4: 10-119676719-A-G
MyVariant Identifiers: chr10:g.121436231A>G (hg19) chr10:g.119676719A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676719A>G , CM000672.2:g.119676719A>G GRCh38
NC_000010.10:g.121436231A>G , CM000672.1:g.121436231A>G GRCh37
NC_000010.9:g.121426221A>G NCBI36
NG_016125.1:g.30350A>G , LRG_742:g.30350A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1165A>G MANE Select ENSP00000358081.4:p.Ser389Gly
ENST00000369085.7:c.1165A>G ENSP00000358081.3:p.Ser389Gly
NM_004281.3:c.1165A>G , LRG_742t1:c.1165A>G NP_004272.2:p.Ser389Gly
XM_005270287.1:c.1162A>G XP_005270344.1:p.Ser388Gly
XM_005270287.2:c.1162A>G XP_005270344.1:p.Ser388Gly
NM_004281.4:c.1165A>G MANE Select NP_004272.2:p.Ser389Gly
Search 100 bp 5'
Search 100 bp 3'