Canonical Allele Identifier: CA596322934
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs998256411
gnomAD v2: 10-121410909-G-C
gnomAD v3: 10-119651397-G-C
gnomAD v4: 10-119651397-G-C
MyVariant Identifiers: chr10:g.121410909G>C (hg19) chr10:g.119651397G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651397G>C , CM000672.2:g.119651397G>C GRCh38
NC_000010.10:g.121410909G>C , CM000672.1:g.121410909G>C GRCh37
NC_000010.9:g.121400899G>C NCBI36
NG_016125.1:g.5028G>C , LRG_742:g.5028G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.-279G>C MANE Select ENSP00000358081.4:n.-279G>C
ENST00000369085.7:c.-279G>C ENSP00000358081.3:n.-279G>C
NM_004281.3:c.-279G>C , LRG_742t1:c.-279G>C NP_004272.2:n.-279G>C
XM_005270287.1:c.-279G>C XP_005270344.1:n.-279G>C
XM_005270287.2:c.-279G>C XP_005270344.1:n.-279G>C
NM_004281.4:c.-279G>C MANE Select NP_004272.2:n.-279G>C
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