Canonical Allele Identifier: CA471739330
Gene: BAG3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121436236G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676724G>A , CM000672.2:g.119676724G>A GRCh38
NC_000010.10:g.121436236G>A , CM000672.1:g.121436236G>A GRCh37
NC_000010.9:g.121426226G>A NCBI36
NG_016125.1:g.30355G>A , LRG_742:g.30355G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1170G>A MANE Select ENSP00000358081.4:p.Val390=
ENST00000369085.7:c.1170G>A ENSP00000358081.3:p.Val390=
NM_004281.3:c.1170G>A , LRG_742t1:c.1170G>A NP_004272.2:p.Val390=
XM_005270287.1:c.1167G>A XP_005270344.1:p.Val389=
XM_005270287.2:c.1167G>A XP_005270344.1:p.Val389=
NM_004281.4:c.1170G>A MANE Select NP_004272.2:p.Val390=