Canonical Allele Identifier: CA471740254
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121432096A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672584A>T , CM000672.2:g.119672584A>T GRCh38
NC_000010.10:g.121432096A>T , CM000672.1:g.121432096A>T GRCh37
NC_000010.9:g.121422086A>T NCBI36
NG_016125.1:g.26215A>T , LRG_742:g.26215A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.837A>T MANE Select ENSP00000358081.4:p.Ser279=
ENST00000369085.7:c.837A>T ENSP00000358081.3:p.Ser279=
ENST00000450186.1:c.663A>T ENSP00000410036.1:p.Ser221=
NM_004281.3:c.837A>T , LRG_742t1:c.837A>T NP_004272.2:p.Ser279=
XM_005270287.1:c.837A>T XP_005270344.1:p.Ser279=
XM_005270287.2:c.837A>T XP_005270344.1:p.Ser279=
NM_004281.4:c.837A>T MANE Select NP_004272.2:p.Ser279=