Canonical Allele Identifier: CA2611160082
Gene: BAG3 HGNC NCBI

Linked Data

gnomAD v4: 10-119672204-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672204G>C , CM000672.2:g.119672204G>C GRCh38
NC_000010.10:g.121431716G>C , CM000672.1:g.121431716G>C GRCh37
NC_000010.9:g.121421706G>C NCBI36
NG_016125.1:g.25835G>C , LRG_742:g.25835G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.508-51G>C MANE Select ENSP00000358081.4:n.508-51G>C
ENST00000369085.7:c.508-51G>C ENSP00000358081.3:n.508-51G>C
ENST00000450186.1:c.334-51G>C ENSP00000410036.1:n.334-51G>C
NM_004281.3:c.508-51G>C , LRG_742t1:c.508-51G>C NP_004272.2:n.508-51G>C
XM_005270287.1:c.508-51G>C XP_005270344.1:n.508-51G>C
XM_005270287.2:c.508-51G>C XP_005270344.1:n.508-51G>C
NM_004281.4:c.508-51G>C MANE Select NP_004272.2:n.508-51G>C
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