Canonical Allele Identifier: CA214221464
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs539119843

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672097C>G , CM000672.2:g.119672097C>G GRCh38
NC_000010.10:g.121431609C>G , CM000672.1:g.121431609C>G GRCh37
NC_000010.9:g.121421599C>G NCBI36
NG_016125.1:g.25728C>G , LRG_742:g.25728C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.508-158C>G MANE Select ENSP00000358081.4:n.508-158C>G
ENST00000369085.7:c.508-158C>G ENSP00000358081.3:n.508-158C>G
ENST00000450186.1:c.334-158C>G ENSP00000410036.1:n.334-158C>G
NM_004281.3:c.508-158C>G , LRG_742t1:c.508-158C>G NP_004272.2:n.508-158C>G
XM_005270287.1:c.508-158C>G XP_005270344.1:n.508-158C>G
XM_005270287.2:c.508-158C>G XP_005270344.1:n.508-158C>G
NM_004281.4:c.508-158C>G MANE Select NP_004272.2:n.508-158C>G