Canonical Allele Identifier: CA2611158935
Gene: BAG3 HGNC NCBI

Linked Data

gnomAD v4: 10-119651393-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651393G>C , CM000672.2:g.119651393G>C GRCh38
NC_000010.10:g.121410905G>C , CM000672.1:g.121410905G>C GRCh37
NC_000010.9:g.121400895G>C NCBI36
NG_016125.1:g.5024G>C , LRG_742:g.5024G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.-283G>C MANE Select ENSP00000358081.4:n.-283G>C
ENST00000369085.7:c.-283G>C ENSP00000358081.3:n.-283G>C
NM_004281.3:c.-283G>C , LRG_742t1:c.-283G>C NP_004272.2:n.-283G>C
XM_005270287.1:c.-283G>C XP_005270344.1:n.-283G>C
XM_005270287.2:c.-283G>C XP_005270344.1:n.-283G>C
NM_004281.4:c.-283G>C MANE Select NP_004272.2:n.-283G>C
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