Canonical Allele Identifier: CA378294916
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121429534G>A (hg19) chr10:g.119670022G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670022G>A , CM000672.2:g.119670022G>A GRCh38
NC_000010.10:g.121429534G>A , CM000672.1:g.121429534G>A GRCh37
NC_000010.9:g.121419524G>A NCBI36
NG_016125.1:g.23653G>A , LRG_742:g.23653G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.352G>A MANE Select ENSP00000358081.4:p.Gly118Arg
ENST00000369085.7:c.352G>A ENSP00000358081.3:p.Gly118Arg
ENST00000450186.1:c.178G>A ENSP00000410036.1:p.Gly60Arg
NM_004281.3:c.352G>A , LRG_742t1:c.352G>A NP_004272.2:p.Gly118Arg
XM_005270287.1:c.352G>A XP_005270344.1:p.Gly118Arg
XM_005270287.2:c.352G>A XP_005270344.1:p.Gly118Arg
NM_004281.4:c.352G>A MANE Select NP_004272.2:p.Gly118Arg
Search 100 bp 5'
Search 100 bp 3'