Canonical Allele Identifier: CA10635035
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 298954
ClinVar RCV Id: RCV000276514 RCV000389524
dbSNP Id: rs879223257
gnomAD v3: 10-119651589-G-T
gnomAD v4: 10-119651589-G-T
MyVariant Identifiers: chr10:g.121411101G>T (hg19) chr10:g.119651589G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651589G>T , CM000672.2:g.119651589G>T GRCh38
NC_000010.10:g.121411101G>T , CM000672.1:g.121411101G>T GRCh37
NC_000010.9:g.121401091G>T NCBI36
NG_016125.1:g.5220G>T , LRG_742:g.5220G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.-87G>T MANE Select ENSP00000358081.4:n.-87G>T
ENST00000369085.7:c.-87G>T ENSP00000358081.3:n.-87G>T
NM_004281.3:c.-87G>T , LRG_742t1:c.-87G>T NP_004272.2:n.-87G>T
XM_005270287.1:c.-87G>T XP_005270344.1:n.-87G>T
XM_005270287.2:c.-87G>T XP_005270344.1:n.-87G>T
NM_004281.4:c.-87G>T MANE Select NP_004272.2:n.-87G>T
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