Canonical Allele Identifier: CA471634423
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1847120299
MyVariant Identifiers: chr10:g.121429405A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669893A>C , CM000672.2:g.119669893A>C GRCh38
NC_000010.10:g.121429405A>C , CM000672.1:g.121429405A>C GRCh37
NC_000010.9:g.121419395A>C NCBI36
NG_016125.1:g.23524A>C , LRG_742:g.23524A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.223A>C MANE Select ENSP00000358081.4:p.Arg75=
ENST00000369085.7:c.223A>C ENSP00000358081.3:p.Arg75=
ENST00000450186.1:c.49A>C ENSP00000410036.1:p.Arg17=
NM_004281.3:c.223A>C , LRG_742t1:c.223A>C NP_004272.2:p.Arg75=
XM_005270287.1:c.223A>C XP_005270344.1:p.Arg75=
XM_005270287.2:c.223A>C XP_005270344.1:p.Arg75=
NM_004281.4:c.223A>C MANE Select NP_004272.2:p.Arg75=