Canonical Allele Identifier: CA471739488
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1457879480
gnomAD v2: 10-121436542-A-G
gnomAD v4: 10-119677030-A-G
MyVariant Identifiers: chr10:g.121436542A>G (hg19) chr10:g.119677030A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677030A>G , CM000672.2:g.119677030A>G GRCh38
NC_000010.10:g.121436542A>G , CM000672.1:g.121436542A>G GRCh37
NC_000010.9:g.121426532A>G NCBI36
NG_016125.1:g.30661A>G , LRG_742:g.30661A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1476A>G MANE Select ENSP00000358081.4:p.Glu492=
ENST00000369085.7:c.1476A>G ENSP00000358081.3:p.Glu492=
NM_004281.3:c.1476A>G , LRG_742t1:c.1476A>G NP_004272.2:p.Glu492=
XM_005270287.1:c.1473A>G XP_005270344.1:p.Glu491=
XM_005270287.2:c.1473A>G XP_005270344.1:p.Glu491=
NM_004281.4:c.1476A>G MANE Select NP_004272.2:p.Glu492=
Search 100 bp 5'
Search 100 bp 3'