Canonical Allele Identifier: CA2611159869
Gene: BAG3 HGNC NCBI

Linked Data

gnomAD v4: 10-119670215-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670215A>C , CM000672.2:g.119670215A>C GRCh38
NC_000010.10:g.121429727A>C , CM000672.1:g.121429727A>C GRCh37
NC_000010.9:g.121419717A>C NCBI36
NG_016125.1:g.23846A>C , LRG_742:g.23846A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.507+38A>C MANE Select ENSP00000358081.4:n.507+38A>C
ENST00000369085.7:c.507+38A>C ENSP00000358081.3:n.507+38A>C
ENST00000450186.1:c.333+38A>C ENSP00000410036.1:n.333+38A>C
NM_004281.3:c.507+38A>C , LRG_742t1:c.507+38A>C NP_004272.2:n.507+38A>C
XM_005270287.1:c.507+38A>C XP_005270344.1:n.507+38A>C
XM_005270287.2:c.507+38A>C XP_005270344.1:n.507+38A>C
NM_004281.4:c.507+38A>C MANE Select NP_004272.2:n.507+38A>C
Search 100 bp 5'
Search 100 bp 3'