Canonical Allele Identifier: CA2740093562
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2951906
ClinVar RCV Id: RCV003812593
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672667T>A , CM000672.2:g.119672667T>A GRCh38
NC_000010.10:g.121432179T>A , CM000672.1:g.121432179T>A GRCh37
NC_000010.9:g.121422169T>A NCBI36
NG_016125.1:g.26298T>A , LRG_742:g.26298T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.909+11T>A MANE Select ENSP00000358081.4:n.909+11T>A
ENST00000369085.7:c.909+11T>A ENSP00000358081.3:n.909+11T>A
ENST00000450186.1:c.735+11T>A ENSP00000410036.1:n.735+11T>A
NM_004281.3:c.909+11T>A , LRG_742t1:c.909+11T>A NP_004272.2:n.909+11T>A
XM_005270287.1:c.909+11T>A XP_005270344.1:n.909+11T>A
XM_005270287.2:c.909+11T>A XP_005270344.1:n.909+11T>A
NM_004281.4:c.909+11T>A MANE Select NP_004272.2:n.909+11T>A
Search 100 bp 5'
Search 100 bp 3'