Canonical Allele Identifier: CA214207804
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs185840368
gnomAD v3: 10-119651585-A-G
gnomAD v4: 10-119651585-A-G
MyVariant Identifiers: chr10:g.121411097A>G (hg19) chr10:g.119651585A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651585A>G , CM000672.2:g.119651585A>G GRCh38
NC_000010.10:g.121411097A>G , CM000672.1:g.121411097A>G GRCh37
NC_000010.9:g.121401087A>G NCBI36
NG_016125.1:g.5216A>G , LRG_742:g.5216A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.-91A>G MANE Select ENSP00000358081.4:n.-91A>G
ENST00000369085.7:c.-91A>G ENSP00000358081.3:n.-91A>G
NM_004281.3:c.-91A>G , LRG_742t1:c.-91A>G NP_004272.2:n.-91A>G
XM_005270287.1:c.-91A>G XP_005270344.1:n.-91A>G
XM_005270287.2:c.-91A>G XP_005270344.1:n.-91A>G
NM_004281.4:c.-91A>G MANE Select NP_004272.2:n.-91A>G
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