Canonical Allele Identifier: CA259788
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 30396
dbSNP Id: rs387906874

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669881C>T , CM000672.2:g.119669881C>T GRCh38
NC_000010.10:g.121429393C>T , CM000672.1:g.121429393C>T GRCh37
NC_000010.9:g.121419383C>T NCBI36
NG_016125.1:g.23512C>T , LRG_742:g.23512C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.211C>T MANE Select ENSP00000358081.4:p.Arg71Trp
ENST00000369085.7:c.211C>T ENSP00000358081.3:p.Arg71Trp
ENST00000450186.1:c.37C>T ENSP00000410036.1:p.Arg13Trp
NM_004281.3:c.211C>T , LRG_742t1:c.211C>T NP_004272.2:p.Arg71Trp
XM_005270287.1:c.211C>T XP_005270344.1:p.Arg71Trp
XM_005270287.2:c.211C>T XP_005270344.1:p.Arg71Trp
NM_004281.4:c.211C>T MANE Select NP_004272.2:p.Arg71Trp