Canonical Allele Identifier: CA378297544
Gene: BAG3 HGNC NCBI

Linked Data

gnomAD v4: 10-119677093-C-G
MyVariant Identifiers: chr10:g.121436605C>G (hg19) chr10:g.119677093C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677093C>G , CM000672.2:g.119677093C>G GRCh38
NC_000010.10:g.121436605C>G , CM000672.1:g.121436605C>G GRCh37
NC_000010.9:g.121426595C>G NCBI36
NG_016125.1:g.30724C>G , LRG_742:g.30724C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1539C>G MANE Select ENSP00000358081.4:p.Ser513Arg
ENST00000369085.7:c.1539C>G ENSP00000358081.3:p.Ser513Arg
NM_004281.3:c.1539C>G , LRG_742t1:c.1539C>G NP_004272.2:p.Ser513Arg
XM_005270287.1:c.1536C>G XP_005270344.1:p.Ser512Arg
XM_005270287.2:c.1536C>G XP_005270344.1:p.Ser512Arg
NM_004281.4:c.1539C>G MANE Select NP_004272.2:p.Ser513Arg
Search 100 bp 5'
Search 100 bp 3'