Canonical Allele Identifier: CA660668979

Gene: BAG3

Linked Data

• dbSNP Id: rs766749403
• MyVariant Identifiers: chr10:g.121411159G>C (hg19) ; chr10:g.119651647G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119651647G>C , CM000672.2:g.119651647G>C	GRCh38
NC_000010.10:g.121411159G>C , CM000672.1:g.121411159G>C	GRCh37
NC_000010.9:g.121401149G>C	NCBI36
NG_016125.1:g.5278G>C , LRG_742:g.5278G>C

Transcript Alleles

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