Canonical Allele Identifier: CA378295484
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121431896G>C (hg19) chr10:g.119672384G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672384G>C , CM000672.2:g.119672384G>C GRCh38
NC_000010.10:g.121431896G>C , CM000672.1:g.121431896G>C GRCh37
NC_000010.9:g.121421886G>C NCBI36
NG_016125.1:g.26015G>C , LRG_742:g.26015G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.637G>C MANE Select ENSP00000358081.4:p.Glu213Gln
ENST00000369085.7:c.637G>C ENSP00000358081.3:p.Glu213Gln
ENST00000450186.1:c.463G>C ENSP00000410036.1:p.Glu155Gln
NM_004281.3:c.637G>C , LRG_742t1:c.637G>C NP_004272.2:p.Glu213Gln
XM_005270287.1:c.637G>C XP_005270344.1:p.Glu213Gln
XM_005270287.2:c.637G>C XP_005270344.1:p.Glu213Gln
NM_004281.4:c.637G>C MANE Select NP_004272.2:p.Glu213Gln
Search 100 bp 5'
Search 100 bp 3'