Canonical Allele Identifier: CA16613029
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 410239
ClinVar RCV Id: RCV000458004
dbSNP Id: rs117749531

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676794G>T , CM000672.2:g.119676794G>T GRCh38
NC_000010.10:g.121436306G>T , CM000672.1:g.121436306G>T GRCh37
NC_000010.9:g.121426296G>T NCBI36
NG_016125.1:g.30425G>T , LRG_742:g.30425G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1240G>T MANE Select ENSP00000358081.4:p.Glu414Ter
ENST00000369085.7:c.1240G>T ENSP00000358081.3:p.Glu414Ter
NM_004281.3:c.1240G>T , LRG_742t1:c.1240G>T NP_004272.2:p.Glu414Ter
XM_005270287.1:c.1237G>T XP_005270344.1:p.Glu413Ter
XM_005270287.2:c.1237G>T XP_005270344.1:p.Glu413Ter
NM_004281.4:c.1240G>T MANE Select NP_004272.2:p.Glu414Ter