Canonical Allele Identifier: CA398519848
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1998506
ClinVar RCV Id: RCV002810510
dbSNP Id: rs2087567198
gnomAD v4: 17-16948792-C-T
COSMIC: COSM3514693 COSM4892255
MyVariant Identifiers: chr17:g.16852106C>T (hg19) chr17:g.16948792C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948792C>T , CM000679.2:g.16948792C>T GRCh38
NC_000017.10:g.16852106C>T , CM000679.1:g.16852106C>T GRCh37
NC_000017.9:g.16792831C>T NCBI36
NG_007281.1:g.28297G>A , LRG_120:g.28297G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.391G>A MANE Select ENSP00000261652.2:p.Asp131Asn
ENST00000261652.6:c.391G>A ENSP00000261652.2:p.Asp131Asn
ENST00000579315.5:c.391G>A ENSP00000464069.1:p.Asp131Asn
ENST00000581616.2:n.394G>A
ENST00000582931.5:n.295G>A
ENST00000583789.1:c.253G>A ENSP00000462952.1:p.Asp85Asn
ENST00000584950.5:c.253G>A ENSP00000463582.1:p.Asp85Asn
NM_012452.2:c.391G>A , LRG_120t1:c.391G>A NP_036584.1:p.Asp131Asn
NM_012452.3:c.391G>A MANE Select NP_036584.1:p.Asp131Asn
Search 100 bp 5'
Search 100 bp 3'