Canonical Allele Identifier: CA471634810
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121436041A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676529A>G , CM000672.2:g.119676529A>G GRCh38
NC_000010.10:g.121436041A>G , CM000672.1:g.121436041A>G GRCh37
NC_000010.9:g.121426031A>G NCBI36
NG_016125.1:g.30160A>G , LRG_742:g.30160A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.975A>G MANE Select ENSP00000358081.4:p.Pro325=
ENST00000369085.7:c.975A>G ENSP00000358081.3:p.Pro325=
ENST00000450186.1:c.798A>G ENSP00000410036.1:p.Pro266=
NM_004281.3:c.975A>G , LRG_742t1:c.975A>G NP_004272.2:p.Pro325=
XM_005270287.1:c.972A>G XP_005270344.1:p.Pro324=
XM_005270287.2:c.972A>G XP_005270344.1:p.Pro324=
NM_004281.4:c.975A>G MANE Select NP_004272.2:p.Pro325=