Canonical Allele Identifier: CA2636329570
Gene: TNFRSF13B HGNC NCBI

Linked Data

gnomAD v4: 17-16948780-T-TGTCTGAATTG
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948780_16948781insGTCTGAATTG , CM000679.2:g.16948780_16948781insGTCTGAATTG GRCh38
NC_000017.10:g.16852094_16852095insGTCTGAATTG , CM000679.1:g.16852094_16852095insGTCTGAATTG GRCh37
NC_000017.9:g.16792819_16792820insGTCTGAATTG NCBI36
NG_007281.1:g.28308_28309insCAATTCAGAC , LRG_120:g.28308_28309insCAATTCAGAC

Transcript Alleles

HGVS Amino-acid change
ENST00000261652.7:c.402_403insCAATTCAGAC MANE Select ENSP00000261652.2:p.Arg135GlnfsTer?
ENST00000261652.6:c.402_403insCAATTCAGAC ENSP00000261652.2:p.Arg135GlnfsTer?
ENST00000579315.5:c.402_403insCAATTCAGAC ENSP00000464069.1:p.Arg135GlnfsTer?
ENST00000581616.2:n.405_406insCAATTCAGAC
ENST00000582931.5:n.306_307insCAATTCAGAC
ENST00000583789.1:c.264_265insCAATTCAGAC ENSP00000462952.1:p.Arg89GlnfsTer?
ENST00000584950.5:c.264_265insCAATTCAGAC ENSP00000463582.1:p.Arg89GlnfsTer?
NM_012452.2:c.402_403insCAATTCAGAC , LRG_120t1:c.402_403insCAATTCAGAC NP_036584.1:p.Arg135GlnfsTer?
NM_012452.3:c.402_403insCAATTCAGAC MANE Select NP_036584.1:p.Arg135GlnfsTer?
Search 100 bp 5'
Search 100 bp 3'