Canonical Allele Identifier: CA214220089
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1739609
ClinVar RCV Id: RCV003094639 RCV002331946
dbSNP Id: rs774506265
gnomAD v2: 10-121429612-A-G
gnomAD v3: 10-119670100-A-G
gnomAD v4: 10-119670100-A-G
MyVariant Identifiers: chr10:g.121429612A>G (hg19) chr10:g.119670100A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670100A>G , CM000672.2:g.119670100A>G GRCh38
NC_000010.10:g.121429612A>G , CM000672.1:g.121429612A>G GRCh37
NC_000010.9:g.121419602A>G NCBI36
NG_016125.1:g.23731A>G , LRG_742:g.23731A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.430A>G MANE Select ENSP00000358081.4:p.Thr144Ala
ENST00000369085.7:c.430A>G ENSP00000358081.3:p.Thr144Ala
ENST00000450186.1:c.256A>G ENSP00000410036.1:p.Thr86Ala
NM_004281.3:c.430A>G , LRG_742t1:c.430A>G NP_004272.2:p.Thr144Ala
XM_005270287.1:c.430A>G XP_005270344.1:p.Thr144Ala
XM_005270287.2:c.430A>G XP_005270344.1:p.Thr144Ala
NM_004281.4:c.430A>G MANE Select NP_004272.2:p.Thr144Ala
Search 100 bp 5'
Search 100 bp 3'