Canonical Allele Identifier: CA471739481
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202554
ClinVar RCV Id: RCV002648049
dbSNP Id: rs1337912162

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676856G>T , CM000672.2:g.119676856G>T GRCh38
NC_000010.10:g.121436368G>T , CM000672.1:g.121436368G>T GRCh37
NC_000010.9:g.121426358G>T NCBI36
NG_016125.1:g.30487G>T , LRG_742:g.30487G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1302G>T MANE Select ENSP00000358081.4:p.Gly434=
ENST00000369085.7:c.1302G>T ENSP00000358081.3:p.Gly434=
NM_004281.3:c.1302G>T , LRG_742t1:c.1302G>T NP_004272.2:p.Gly434=
XM_005270287.1:c.1299G>T XP_005270344.1:p.Gly433=
XM_005270287.2:c.1299G>T XP_005270344.1:p.Gly433=
NM_004281.4:c.1302G>T MANE Select NP_004272.2:p.Gly434=