Canonical Allele Identifier: CA660668887
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1429748103
gnomAD v3: 10-119651453-C-G
gnomAD v4: 10-119651453-C-G
MyVariant Identifiers: chr10:g.121410965C>G (hg19) chr10:g.119651453C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651453C>G , CM000672.2:g.119651453C>G GRCh38
NC_000010.10:g.121410965C>G , CM000672.1:g.121410965C>G GRCh37
NC_000010.9:g.121400955C>G NCBI36
NG_016125.1:g.5084C>G , LRG_742:g.5084C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.-223C>G MANE Select ENSP00000358081.4:n.-223C>G
ENST00000369085.7:c.-223C>G ENSP00000358081.3:n.-223C>G
NM_004281.3:c.-223C>G , LRG_742t1:c.-223C>G NP_004272.2:n.-223C>G
XM_005270287.1:c.-223C>G XP_005270344.1:n.-223C>G
XM_005270287.2:c.-223C>G XP_005270344.1:n.-223C>G
NM_004281.4:c.-223C>G MANE Select NP_004272.2:n.-223C>G
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