Canonical Allele Identifier: CA471634519
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121429536G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670024G>T , CM000672.2:g.119670024G>T GRCh38
NC_000010.10:g.121429536G>T , CM000672.1:g.121429536G>T GRCh37
NC_000010.9:g.121419526G>T NCBI36
NG_016125.1:g.23655G>T , LRG_742:g.23655G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.354G>T MANE Select ENSP00000358081.4:p.Gly118=
ENST00000369085.7:c.354G>T ENSP00000358081.3:p.Gly118=
ENST00000450186.1:c.180G>T ENSP00000410036.1:p.Gly60=
NM_004281.3:c.354G>T , LRG_742t1:c.354G>T NP_004272.2:p.Gly118=
XM_005270287.1:c.354G>T XP_005270344.1:p.Gly118=
XM_005270287.2:c.354G>T XP_005270344.1:p.Gly118=
NM_004281.4:c.354G>T MANE Select NP_004272.2:p.Gly118=