Canonical Allele Identifier: CA660673481
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1267016210
MyVariant Identifiers: chr10:g.121429320C>A (hg19) chr10:g.119669808C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669808C>A , CM000672.2:g.119669808C>A GRCh38
NC_000010.10:g.121429320C>A , CM000672.1:g.121429320C>A GRCh37
NC_000010.9:g.121419310C>A NCBI36
NG_016125.1:g.23439C>A , LRG_742:g.23439C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.181-43C>A MANE Select ENSP00000358081.4:n.181-43C>A
ENST00000369085.7:c.181-43C>A ENSP00000358081.3:n.181-43C>A
ENST00000450186.1:c.7-43C>A ENSP00000410036.1:n.7-43C>A
NM_004281.3:c.181-43C>A , LRG_742t1:c.181-43C>A NP_004272.2:n.181-43C>A
XM_005270287.1:c.181-43C>A XP_005270344.1:n.181-43C>A
XM_005270287.2:c.181-43C>A XP_005270344.1:n.181-43C>A
NM_004281.4:c.181-43C>A MANE Select NP_004272.2:n.181-43C>A
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