Canonical Allele Identifier: CA5716201
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs752723601
ExAC: 10:121411175 A / T
gnomAD v2: 10-121411175-A-T
gnomAD v4: 10-119651663-A-T
MyVariant Identifiers: chr10:g.121411175A>T (hg19) chr10:g.121411175_121411176delinsTC (hg19) chr10:g.119651663A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651663A>T , CM000672.2:g.119651663A>T GRCh38
NC_000010.10:g.121411175A>T , CM000672.1:g.121411175A>T GRCh37
NC_000010.9:g.121401165A>T NCBI36
NG_016125.1:g.5294A>T , LRG_742:g.5294A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.-13A>T MANE Select ENSP00000358081.4:n.-13A>T
ENST00000369085.7:c.-13A>T ENSP00000358081.3:n.-13A>T
NM_004281.3:c.-13A>T , LRG_742t1:c.-13A>T NP_004272.2:n.-13A>T
XM_005270287.1:c.-13A>T XP_005270344.1:n.-13A>T
XM_005270287.2:c.-13A>T XP_005270344.1:n.-13A>T
NM_004281.4:c.-13A>T MANE Select NP_004272.2:n.-13A>T
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