Canonical Allele Identifier: CA214207624
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs2736419
gnomAD v3: 10-119651408-C-T
gnomAD v4: 10-119651408-C-T
MyVariant Identifiers: chr10:g.121410920C>T (hg19) chr10:g.119651408C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651408C>T , CM000672.2:g.119651408C>T GRCh38
NC_000010.10:g.121410920C>T , CM000672.1:g.121410920C>T GRCh37
NC_000010.9:g.121400910C>T NCBI36
NG_016125.1:g.5039C>T , LRG_742:g.5039C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.-268C>T MANE Select ENSP00000358081.4:n.-268C>T
ENST00000369085.7:c.-268C>T ENSP00000358081.3:n.-268C>T
NM_004281.3:c.-268C>T , LRG_742t1:c.-268C>T NP_004272.2:n.-268C>T
XM_005270287.1:c.-268C>T XP_005270344.1:n.-268C>T
XM_005270287.2:c.-268C>T XP_005270344.1:n.-268C>T
NM_004281.4:c.-268C>T MANE Select NP_004272.2:n.-268C>T
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