Canonical Allele Identifier: CA471634486
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121429482T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669970T>C , CM000672.2:g.119669970T>C GRCh38
NC_000010.10:g.121429482T>C , CM000672.1:g.121429482T>C GRCh37
NC_000010.9:g.121419472T>C NCBI36
NG_016125.1:g.23601T>C , LRG_742:g.23601T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.300T>C MANE Select ENSP00000358081.4:p.His100=
ENST00000369085.7:c.300T>C ENSP00000358081.3:p.His100=
ENST00000450186.1:c.126T>C ENSP00000410036.1:p.His42=
NM_004281.3:c.300T>C , LRG_742t1:c.300T>C NP_004272.2:p.His100=
XM_005270287.1:c.300T>C XP_005270344.1:p.His100=
XM_005270287.2:c.300T>C XP_005270344.1:p.His100=
NM_004281.4:c.300T>C MANE Select NP_004272.2:p.His100=
Search 100 bp 5'
Search 100 bp 3'