Canonical Allele Identifier: CA660663634

Gene: BAG3

Linked Data

• dbSNP Id: rs1291480597
• gnomAD v4: 10-119670242-C-T
• MyVariant Identifiers: chr10:g.121429754C>T (hg19) ; chr10:g.119670242C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119670242C>T , CM000672.2:g.119670242C>T	GRCh38
NC_000010.10:g.121429754C>T , CM000672.1:g.121429754C>T	GRCh37
NC_000010.9:g.121419744C>T	NCBI36
NG_016125.1:g.23873C>T , LRG_742:g.23873C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.507+65C>T MANE Select	ENSP00000358081.4:n.507+65C>T
ENST00000369085.7:c.507+65C>T	ENSP00000358081.3:n.507+65C>T
ENST00000450186.1:c.333+65C>T	ENSP00000410036.1:n.333+65C>T
NM_004281.3:c.507+65C>T , LRG_742t1:c.507+65C>T	NP_004272.2:n.507+65C>T
XM_005270287.1:c.507+65C>T	XP_005270344.1:n.507+65C>T
XM_005270287.2:c.507+65C>T	XP_005270344.1:n.507+65C>T
NM_004281.4:c.507+65C>T MANE Select	NP_004272.2:n.507+65C>T