Canonical Allele Identifier: CA214222103
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 427243
ClinVar RCV Id: RCV000490546
dbSNP Id: rs751261054
MyVariant Identifiers: chr10:g.121432095C>A (hg19) chr10:g.119672583C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672583C>A , CM000672.2:g.119672583C>A GRCh38
NC_000010.10:g.121432095C>A , CM000672.1:g.121432095C>A GRCh37
NC_000010.9:g.121422085C>A NCBI36
NG_016125.1:g.26214C>A , LRG_742:g.26214C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.836C>A MANE Select ENSP00000358081.4:p.Ser279Ter
ENST00000369085.7:c.836C>A ENSP00000358081.3:p.Ser279Ter
ENST00000450186.1:c.662C>A ENSP00000410036.1:p.Ser221Ter
NM_004281.3:c.836C>A , LRG_742t1:c.836C>A NP_004272.2:p.Ser279Ter
XM_005270287.1:c.836C>A XP_005270344.1:p.Ser279Ter
XM_005270287.2:c.836C>A XP_005270344.1:p.Ser279Ter
NM_004281.4:c.836C>A MANE Select NP_004272.2:p.Ser279Ter
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