Canonical Allele Identifier: CA471739338
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2941671
ClinVar RCV Id: RCV003802693
MyVariant Identifiers: chr10:g.121436239T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676727T>G , CM000672.2:g.119676727T>G GRCh38
NC_000010.10:g.121436239T>G , CM000672.1:g.121436239T>G GRCh37
NC_000010.9:g.121426229T>G NCBI36
NG_016125.1:g.30358T>G , LRG_742:g.30358T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1173T>G MANE Select ENSP00000358081.4:p.Ala391=
ENST00000369085.7:c.1173T>G ENSP00000358081.3:p.Ala391=
NM_004281.3:c.1173T>G , LRG_742t1:c.1173T>G NP_004272.2:p.Ala391=
XM_005270287.1:c.1170T>G XP_005270344.1:p.Ala390=
XM_005270287.2:c.1170T>G XP_005270344.1:p.Ala390=
NM_004281.4:c.1173T>G MANE Select NP_004272.2:p.Ala391=