Canonical Allele Identifier: CA471634447
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121429434T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669922T>G , CM000672.2:g.119669922T>G GRCh38
NC_000010.10:g.121429434T>G , CM000672.1:g.121429434T>G GRCh37
NC_000010.9:g.121419424T>G NCBI36
NG_016125.1:g.23553T>G , LRG_742:g.23553T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.252T>G MANE Select ENSP00000358081.4:p.Pro84=
ENST00000369085.7:c.252T>G ENSP00000358081.3:p.Pro84=
ENST00000450186.1:c.78T>G ENSP00000410036.1:p.Pro26=
NM_004281.3:c.252T>G , LRG_742t1:c.252T>G NP_004272.2:p.Pro84=
XM_005270287.1:c.252T>G XP_005270344.1:p.Pro84=
XM_005270287.2:c.252T>G XP_005270344.1:p.Pro84=
NM_004281.4:c.252T>G MANE Select NP_004272.2:p.Pro84=