Canonical Allele Identifier: CA2576183938
Gene: TNFRSF13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948971del , CM000679.2:g.16948971del GRCh38
NC_000017.10:g.16852285del , CM000679.1:g.16852285del GRCh37
NC_000017.9:g.16793010del NCBI36
NG_007281.1:g.28118del , LRG_120:g.28118del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.212del MANE Select ENSP00000261652.2:p.Cys71SerfsTer13
ENST00000261652.6:c.212del ENSP00000261652.2:p.Cys71SerfsTer13
ENST00000579315.5:c.212del ENSP00000464069.1:p.Cys71SerfsTer13
ENST00000581616.2:n.215del
ENST00000582931.5:n.116del
ENST00000583789.1:c.74del ENSP00000462952.1:p.Cys25SerfsTer13
ENST00000584950.5:c.74del ENSP00000463582.1:p.Cys25SerfsTer13
NM_012452.2:c.212del , LRG_120t1:c.212del NP_036584.1:p.Cys71SerfsTer13
NM_012452.3:c.212del MANE Select NP_036584.1:p.Cys71SerfsTer13
Search 100 bp 5'
Search 100 bp 3'