Canonical Allele Identifier: CA596325802

Gene: BAG3

Linked Data

• dbSNP Id: rs1336324632
• gnomAD v2: 10-121429718-C-G
• gnomAD v4: 10-119670206-C-G
• MyVariant Identifiers: chr10:g.121429718C>G (hg19) ; chr10:g.119670206C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119670206C>G , CM000672.2:g.119670206C>G	GRCh38
NC_000010.10:g.121429718C>G , CM000672.1:g.121429718C>G	GRCh37
NC_000010.9:g.121419708C>G	NCBI36
NG_016125.1:g.23837C>G , LRG_742:g.23837C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.507+29C>G MANE Select	ENSP00000358081.4:n.507+29C>G
ENST00000369085.7:c.507+29C>G	ENSP00000358081.3:n.507+29C>G
ENST00000450186.1:c.333+29C>G	ENSP00000410036.1:n.333+29C>G
NM_004281.3:c.507+29C>G , LRG_742t1:c.507+29C>G	NP_004272.2:n.507+29C>G
XM_005270287.1:c.507+29C>G	XP_005270344.1:n.507+29C>G
XM_005270287.2:c.507+29C>G	XP_005270344.1:n.507+29C>G
NM_004281.4:c.507+29C>G MANE Select	NP_004272.2:n.507+29C>G