Canonical Allele Identifier: CA378294181
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121411288C>A (hg19) chr10:g.119651776C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651776C>A , CM000672.2:g.119651776C>A GRCh38
NC_000010.10:g.121411288C>A , CM000672.1:g.121411288C>A GRCh37
NC_000010.9:g.121401278C>A NCBI36
NG_016125.1:g.5407C>A , LRG_742:g.5407C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.101C>A MANE Select ENSP00000358081.4:p.Thr34Asn
ENST00000369085.7:c.101C>A ENSP00000358081.3:p.Thr34Asn
NM_004281.3:c.101C>A , LRG_742t1:c.101C>A NP_004272.2:p.Thr34Asn
XM_005270287.1:c.101C>A XP_005270344.1:p.Thr34Asn
XM_005270287.2:c.101C>A XP_005270344.1:p.Thr34Asn
NM_004281.4:c.101C>A MANE Select NP_004272.2:p.Thr34Asn
Search 100 bp 5'
Search 100 bp 3'