Canonical Allele Identifier: CA378297634
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121436647G>C (hg19) chr10:g.119677135G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677135G>C , CM000672.2:g.119677135G>C GRCh38
NC_000010.10:g.121436647G>C , CM000672.1:g.121436647G>C GRCh37
NC_000010.9:g.121426637G>C NCBI36
NG_016125.1:g.30766G>C , LRG_742:g.30766G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1581G>C MANE Select ENSP00000358081.4:p.Met527Ile
ENST00000369085.7:c.1581G>C ENSP00000358081.3:p.Met527Ile
NM_004281.3:c.1581G>C , LRG_742t1:c.1581G>C NP_004272.2:p.Met527Ile
XM_005270287.1:c.1578G>C XP_005270344.1:p.Met526Ile
XM_005270287.2:c.1578G>C XP_005270344.1:p.Met526Ile
NM_004281.4:c.1581G>C MANE Select NP_004272.2:p.Met527Ile
Search 100 bp 5'
Search 100 bp 3'