Canonical Allele Identifier: CA471633576
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121411196C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651684C>T , CM000672.2:g.119651684C>T GRCh38
NC_000010.10:g.121411196C>T , CM000672.1:g.121411196C>T GRCh37
NC_000010.9:g.121401186C>T NCBI36
NG_016125.1:g.5315C>T , LRG_742:g.5315C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.9C>T MANE Select ENSP00000358081.4:p.Ala3=
ENST00000369085.7:c.9C>T ENSP00000358081.3:p.Ala3=
NM_004281.3:c.9C>T , LRG_742t1:c.9C>T NP_004272.2:p.Ala3=
XM_005270287.1:c.9C>T XP_005270344.1:p.Ala3=
XM_005270287.2:c.9C>T XP_005270344.1:p.Ala3=
NM_004281.4:c.9C>T MANE Select NP_004272.2:p.Ala3=