Canonical Allele Identifier: CA2695201252
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2633419
ClinVar RCV Id: RCV003391570
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948877_16948880delinsCAA , CM000679.2:g.16948877_16948880delinsCAA GRCh38
NC_000017.10:g.16852191_16852194delinsCAA , CM000679.1:g.16852191_16852194delinsCAA GRCh37
NC_000017.9:g.16792916_16792919delinsCAA NCBI36
NG_007281.1:g.28209_28212delinsTTG , LRG_120:g.28209_28212delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.303_306delinsTTG MANE Select ENSP00000261652.2:p.Tyr102CysfsTer11
ENST00000261652.6:c.303_306delinsTTG ENSP00000261652.2:p.Tyr102CysfsTer11
ENST00000579315.5:c.303_306delinsTTG ENSP00000464069.1:p.Tyr102CysfsTer11
ENST00000581616.2:n.306_309delinsTTG
ENST00000582931.5:n.207_210delinsTTG
ENST00000583789.1:c.165_168delinsTTG ENSP00000462952.1:p.Tyr56CysfsTer11
ENST00000584950.5:c.165_168delinsTTG ENSP00000463582.1:p.Tyr56CysfsTer11
NM_012452.2:c.303_306delinsTTG , LRG_120t1:c.303_306delinsTTG NP_036584.1:p.Tyr102CysfsTer11
NM_012452.3:c.303_306delinsTTG MANE Select NP_036584.1:p.Tyr102CysfsTer11
Search 100 bp 5'
Search 100 bp 3'