Canonical Allele Identifier: CA471739754
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1284277
ClinVar RCV Id: RCV001699601 RCV001702247
dbSNP Id: rs2134065088
MyVariant Identifiers: chr10:g.121431871G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672359G>A , CM000672.2:g.119672359G>A GRCh38
NC_000010.10:g.121431871G>A , CM000672.1:g.121431871G>A GRCh37
NC_000010.9:g.121421861G>A NCBI36
NG_016125.1:g.25990G>A , LRG_742:g.25990G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.612G>A MANE Select ENSP00000358081.4:p.Gly204=
ENST00000369085.7:c.612G>A ENSP00000358081.3:p.Gly204=
ENST00000450186.1:c.438G>A ENSP00000410036.1:p.Gly146=
NM_004281.3:c.612G>A , LRG_742t1:c.612G>A NP_004272.2:p.Gly204=
XM_005270287.1:c.612G>A XP_005270344.1:p.Gly204=
XM_005270287.2:c.612G>A XP_005270344.1:p.Gly204=
NM_004281.4:c.612G>A MANE Select NP_004272.2:p.Gly204=
Search 100 bp 5'
Search 100 bp 3'