Canonical Allele Identifier: CA378297031
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769533
ClinVar RCV Id: RCV002380971
MyVariant Identifiers: chr10:g.121436372G>T (hg19) chr10:g.119676860G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676860G>T , CM000672.2:g.119676860G>T GRCh38
NC_000010.10:g.121436372G>T , CM000672.1:g.121436372G>T GRCh37
NC_000010.9:g.121426362G>T NCBI36
NG_016125.1:g.30491G>T , LRG_742:g.30491G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1306G>T MANE Select ENSP00000358081.4:p.Glu436Ter
ENST00000369085.7:c.1306G>T ENSP00000358081.3:p.Glu436Ter
NM_004281.3:c.1306G>T , LRG_742t1:c.1306G>T NP_004272.2:p.Glu436Ter
XM_005270287.1:c.1303G>T XP_005270344.1:p.Glu435Ter
XM_005270287.2:c.1303G>T XP_005270344.1:p.Glu435Ter
NM_004281.4:c.1306G>T MANE Select NP_004272.2:p.Glu436Ter
Search 100 bp 5'
Search 100 bp 3'