Canonical Allele Identifier: CA471634730
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121432132G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672620G>T , CM000672.2:g.119672620G>T GRCh38
NC_000010.10:g.121432132G>T , CM000672.1:g.121432132G>T GRCh37
NC_000010.9:g.121422122G>T NCBI36
NG_016125.1:g.26251G>T , LRG_742:g.26251G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.873G>T MANE Select ENSP00000358081.4:p.Ser291=
ENST00000369085.7:c.873G>T ENSP00000358081.3:p.Ser291=
ENST00000450186.1:c.699G>T ENSP00000410036.1:p.Ser233=
NM_004281.3:c.873G>T , LRG_742t1:c.873G>T NP_004272.2:p.Ser291=
XM_005270287.1:c.873G>T XP_005270344.1:p.Ser291=
XM_005270287.2:c.873G>T XP_005270344.1:p.Ser291=
NM_004281.4:c.873G>T MANE Select NP_004272.2:p.Ser291=