Canonical Allele Identifier: CA256833455
Gene: TNFSF13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108308037T>A , CM000675.2:g.108308037T>A GRCh38
NC_000013.10:g.108960385T>A , CM000675.1:g.108960385T>A GRCh37
NC_000013.9:g.107758386T>A NCBI36
NG_029524.1:g.43409T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375887.9:c.*1099T>A MANE Select ENSP00000365048.3:n.*1099T>A
ENST00000375887.8:c.*1099T>A ENSP00000365048.3:n.*1099T>A
ENST00000430559.5:c.*1099T>A ENSP00000389540.1:n.*1099T>A
NM_001145645.2:c.*1099T>A NP_001139117.1:n.*1099T>A
NM_006573.4:c.*1099T>A NP_006564.1:n.*1099T>A
NM_006573.5:c.*1099T>A MANE Select NP_006564.1:n.*1099T>A
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