Canonical Allele Identifier: CA378295569
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121431937C>A (hg19) chr10:g.119672425C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672425C>A , CM000672.2:g.119672425C>A GRCh38
NC_000010.10:g.121431937C>A , CM000672.1:g.121431937C>A GRCh37
NC_000010.9:g.121421927C>A NCBI36
NG_016125.1:g.26056C>A , LRG_742:g.26056C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.678C>A MANE Select ENSP00000358081.4:p.His226Gln
ENST00000369085.7:c.678C>A ENSP00000358081.3:p.His226Gln
ENST00000450186.1:c.504C>A ENSP00000410036.1:p.His168Gln
NM_004281.3:c.678C>A , LRG_742t1:c.678C>A NP_004272.2:p.His226Gln
XM_005270287.1:c.678C>A XP_005270344.1:p.His226Gln
XM_005270287.2:c.678C>A XP_005270344.1:p.His226Gln
NM_004281.4:c.678C>A MANE Select NP_004272.2:p.His226Gln
Search 100 bp 5'
Search 100 bp 3'