Canonical Allele Identifier: CA378297443
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121436559C>A (hg19) chr10:g.119677047C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677047C>A , CM000672.2:g.119677047C>A GRCh38
NC_000010.10:g.121436559C>A , CM000672.1:g.121436559C>A GRCh37
NC_000010.9:g.121426549C>A NCBI36
NG_016125.1:g.30678C>A , LRG_742:g.30678C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1493C>A MANE Select ENSP00000358081.4:p.Ala498Asp
ENST00000369085.7:c.1493C>A ENSP00000358081.3:p.Ala498Asp
NM_004281.3:c.1493C>A , LRG_742t1:c.1493C>A NP_004272.2:p.Ala498Asp
XM_005270287.1:c.1490C>A XP_005270344.1:p.Ala497Asp
XM_005270287.2:c.1490C>A XP_005270344.1:p.Ala497Asp
NM_004281.4:c.1493C>A MANE Select NP_004272.2:p.Ala498Asp
Search 100 bp 5'
Search 100 bp 3'