Canonical Allele Identifier: CA660673430
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1264385047
gnomAD v3: 10-119669632-T-C
gnomAD v4: 10-119669632-T-C
MyVariant Identifiers: chr10:g.121429144T>C (hg19) chr10:g.119669632T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669632T>C , CM000672.2:g.119669632T>C GRCh38
NC_000010.10:g.121429144T>C , CM000672.1:g.121429144T>C GRCh37
NC_000010.9:g.121419134T>C NCBI36
NG_016125.1:g.23263T>C , LRG_742:g.23263T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.181-219T>C MANE Select ENSP00000358081.4:n.181-219T>C
ENST00000369085.7:c.181-219T>C ENSP00000358081.3:n.181-219T>C
ENST00000450186.1:c.7-219T>C ENSP00000410036.1:n.7-219T>C
NM_004281.3:c.181-219T>C , LRG_742t1:c.181-219T>C NP_004272.2:n.181-219T>C
XM_005270287.1:c.181-219T>C XP_005270344.1:n.181-219T>C
XM_005270287.2:c.181-219T>C XP_005270344.1:n.181-219T>C
NM_004281.4:c.181-219T>C MANE Select NP_004272.2:n.181-219T>C
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