Canonical Allele Identifier: CA378297496
Gene: BAG3 HGNC NCBI

Linked Data

gnomAD v4: 10-119677071-A-G
MyVariant Identifiers: chr10:g.121436583A>G (hg19) chr10:g.119677071A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677071A>G , CM000672.2:g.119677071A>G GRCh38
NC_000010.10:g.121436583A>G , CM000672.1:g.121436583A>G GRCh37
NC_000010.9:g.121426573A>G NCBI36
NG_016125.1:g.30702A>G , LRG_742:g.30702A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1517A>G MANE Select ENSP00000358081.4:p.Gln506Arg
ENST00000369085.7:c.1517A>G ENSP00000358081.3:p.Gln506Arg
NM_004281.3:c.1517A>G , LRG_742t1:c.1517A>G NP_004272.2:p.Gln506Arg
XM_005270287.1:c.1514A>G XP_005270344.1:p.Gln505Arg
XM_005270287.2:c.1514A>G XP_005270344.1:p.Gln505Arg
NM_004281.4:c.1517A>G MANE Select NP_004272.2:p.Gln506Arg
Search 100 bp 5'
Search 100 bp 3'