Canonical Allele Identifier: CA214221886

Gene: BAG3

Linked Data

• dbSNP Id: rs369377620
• MyVariant Identifiers: chr10:g.121431970G>T (hg19) ; chr10:g.119672458G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672458G>T , CM000672.2:g.119672458G>T	GRCh38
NC_000010.10:g.121431970G>T , CM000672.1:g.121431970G>T	GRCh37
NC_000010.9:g.121421960G>T	NCBI36
NG_016125.1:g.26089G>T , LRG_742:g.26089G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.711G>T MANE Select	ENSP00000358081.4:p.Gln237His
ENST00000369085.7:c.711G>T	ENSP00000358081.3:p.Gln237His
ENST00000450186.1:c.537G>T	ENSP00000410036.1:p.Gln179His
NM_004281.3:c.711G>T , LRG_742t1:c.711G>T	NP_004272.2:p.Gln237His
XM_005270287.1:c.711G>T	XP_005270344.1:p.Gln237His
XM_005270287.2:c.711G>T	XP_005270344.1:p.Gln237His
NM_004281.4:c.711G>T MANE Select	NP_004272.2:p.Gln237His