Canonical Allele Identifier: CA471634498
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121429503G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669991G>A , CM000672.2:g.119669991G>A GRCh38
NC_000010.10:g.121429503G>A , CM000672.1:g.121429503G>A GRCh37
NC_000010.9:g.121419493G>A NCBI36
NG_016125.1:g.23622G>A , LRG_742:g.23622G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.321G>A MANE Select ENSP00000358081.4:p.Gln107=
ENST00000369085.7:c.321G>A ENSP00000358081.3:p.Gln107=
ENST00000450186.1:c.147G>A ENSP00000410036.1:p.Gln49=
NM_004281.3:c.321G>A , LRG_742t1:c.321G>A NP_004272.2:p.Gln107=
XM_005270287.1:c.321G>A XP_005270344.1:p.Gln107=
XM_005270287.2:c.321G>A XP_005270344.1:p.Gln107=
NM_004281.4:c.321G>A MANE Select NP_004272.2:p.Gln107=