Canonical Allele Identifier: CA2611160077
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1342352759

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672197A>T , CM000672.2:g.119672197A>T GRCh38
NC_000010.10:g.121431709A>T , CM000672.1:g.121431709A>T GRCh37
NC_000010.9:g.121421699A>T NCBI36
NG_016125.1:g.25828A>T , LRG_742:g.25828A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.508-58A>T MANE Select ENSP00000358081.4:n.508-58A>T
ENST00000369085.7:c.508-58A>T ENSP00000358081.3:n.508-58A>T
ENST00000450186.1:c.334-58A>T ENSP00000410036.1:n.334-58A>T
NM_004281.3:c.508-58A>T , LRG_742t1:c.508-58A>T NP_004272.2:n.508-58A>T
XM_005270287.1:c.508-58A>T XP_005270344.1:n.508-58A>T
XM_005270287.2:c.508-58A>T XP_005270344.1:n.508-58A>T
NM_004281.4:c.508-58A>T MANE Select NP_004272.2:n.508-58A>T