Canonical Allele Identifier: CA2611158954
Gene: BAG3 HGNC NCBI

Linked Data

gnomAD v4: 10-119651407-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651407T>C , CM000672.2:g.119651407T>C GRCh38
NC_000010.10:g.121410919T>C , CM000672.1:g.121410919T>C GRCh37
NC_000010.9:g.121400909T>C NCBI36
NG_016125.1:g.5038T>C , LRG_742:g.5038T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.-269T>C MANE Select ENSP00000358081.4:n.-269T>C
ENST00000369085.7:c.-269T>C ENSP00000358081.3:n.-269T>C
NM_004281.3:c.-269T>C , LRG_742t1:c.-269T>C NP_004272.2:n.-269T>C
XM_005270287.1:c.-269T>C XP_005270344.1:n.-269T>C
XM_005270287.2:c.-269T>C XP_005270344.1:n.-269T>C
NM_004281.4:c.-269T>C MANE Select NP_004272.2:n.-269T>C
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