Canonical Allele Identifier: CA214220431
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs531782527
gnomAD v2: 10-121429778-G-A
gnomAD v3: 10-119670266-G-A
gnomAD v4: 10-119670266-G-A
MyVariant Identifiers: chr10:g.121429778G>A (hg19) chr10:g.119670266G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670266G>A , CM000672.2:g.119670266G>A GRCh38
NC_000010.10:g.121429778G>A , CM000672.1:g.121429778G>A GRCh37
NC_000010.9:g.121419768G>A NCBI36
NG_016125.1:g.23897G>A , LRG_742:g.23897G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.507+89G>A MANE Select ENSP00000358081.4:n.507+89G>A
ENST00000369085.7:c.507+89G>A ENSP00000358081.3:n.507+89G>A
ENST00000450186.1:c.333+89G>A ENSP00000410036.1:n.333+89G>A
NM_004281.3:c.507+89G>A , LRG_742t1:c.507+89G>A NP_004272.2:n.507+89G>A
XM_005270287.1:c.507+89G>A XP_005270344.1:n.507+89G>A
XM_005270287.2:c.507+89G>A XP_005270344.1:n.507+89G>A
NM_004281.4:c.507+89G>A MANE Select NP_004272.2:n.507+89G>A
Search 100 bp 5'
Search 100 bp 3'