Canonical Allele Identifier: CA5716258
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs758106127
ExAC: 10:121429355 T / G
gnomAD v2: 10-121429355-T-G
gnomAD v4: 10-119669843-T-G
MyVariant Identifiers: chr10:g.121429355T>G (hg19) chr10:g.119669843T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669843T>G , CM000672.2:g.119669843T>G GRCh38
NC_000010.10:g.121429355T>G , CM000672.1:g.121429355T>G GRCh37
NC_000010.9:g.121419345T>G NCBI36
NG_016125.1:g.23474T>G , LRG_742:g.23474T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.181-8T>G MANE Select ENSP00000358081.4:n.181-8T>G
ENST00000369085.7:c.181-8T>G ENSP00000358081.3:n.181-8T>G
ENST00000450186.1:c.7-8T>G ENSP00000410036.1:n.7-8T>G
NM_004281.3:c.181-8T>G , LRG_742t1:c.181-8T>G NP_004272.2:n.181-8T>G
XM_005270287.1:c.181-8T>G XP_005270344.1:n.181-8T>G
XM_005270287.2:c.181-8T>G XP_005270344.1:n.181-8T>G
NM_004281.4:c.181-8T>G MANE Select NP_004272.2:n.181-8T>G
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