Canonical Allele Identifier: CA471739151
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121431778T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672266T>G , CM000672.2:g.119672266T>G GRCh38
NC_000010.10:g.121431778T>G , CM000672.1:g.121431778T>G GRCh37
NC_000010.9:g.121421768T>G NCBI36
NG_016125.1:g.25897T>G , LRG_742:g.25897T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.519T>G MANE Select ENSP00000358081.4:p.Ser173=
ENST00000369085.7:c.519T>G ENSP00000358081.3:p.Ser173=
ENST00000450186.1:c.345T>G ENSP00000410036.1:p.Ser115=
NM_004281.3:c.519T>G , LRG_742t1:c.519T>G NP_004272.2:p.Ser173=
XM_005270287.1:c.519T>G XP_005270344.1:p.Ser173=
XM_005270287.2:c.519T>G XP_005270344.1:p.Ser173=
NM_004281.4:c.519T>G MANE Select NP_004272.2:p.Ser173=