Canonical Allele Identifier: CA5716380
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs773557969

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672358G>T , CM000672.2:g.119672358G>T GRCh38
NC_000010.10:g.121431870G>T , CM000672.1:g.121431870G>T GRCh37
NC_000010.9:g.121421860G>T NCBI36
NG_016125.1:g.25989G>T , LRG_742:g.25989G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.611G>T MANE Select ENSP00000358081.4:p.Gly204Val
ENST00000369085.7:c.611G>T ENSP00000358081.3:p.Gly204Val
ENST00000450186.1:c.437G>T ENSP00000410036.1:p.Gly146Val
NM_004281.3:c.611G>T , LRG_742t1:c.611G>T NP_004272.2:p.Gly204Val
XM_005270287.1:c.611G>T XP_005270344.1:p.Gly204Val
XM_005270287.2:c.611G>T XP_005270344.1:p.Gly204Val
NM_004281.4:c.611G>T MANE Select NP_004272.2:p.Gly204Val