Canonical Allele Identifier: CA660668907
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1167348431
gnomAD v3: 10-119651525-AC-A
gnomAD v4: 10-119651525-AC-A
MyVariant Identifiers: chr10:g.121411038del (hg19) chr10:g.119651526del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651530del , CM000672.2:g.119651530del GRCh38
NC_000010.10:g.121411042del , CM000672.1:g.121411042del GRCh37
NC_000010.9:g.121401032del NCBI36
NG_016125.1:g.5161del , LRG_742:g.5161del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.-146del MANE Select ENSP00000358081.4:n.-146del
ENST00000369085.7:c.-146del ENSP00000358081.3:n.-146del
NM_004281.3:c.-146del , LRG_742t1:c.-146del NP_004272.2:n.-146del
XM_005270287.1:c.-146del XP_005270344.1:n.-146del
XM_005270287.2:c.-146del XP_005270344.1:n.-146del
NM_004281.4:c.-146del MANE Select NP_004272.2:n.-146del
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