Canonical Allele Identifier: CA498420343

Gene: TNFRSF13B

Linked Data

• ClinVar Variation Id: 1645260
• ClinVar RCV Id: RCV002148453
• dbSNP Id: rs765245909
• gnomAD v4: 17-16948976-G-T
• MyVariant Identifiers: chr17:g.16852290G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948976G>T , CM000679.2:g.16948976G>T	GRCh38
NC_000017.10:g.16852290G>T , CM000679.1:g.16852290G>T	GRCh37
NC_000017.9:g.16793015G>T	NCBI36
NG_007281.1:g.28113C>A , LRG_120:g.28113C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.207C>A MANE Select	ENSP00000261652.2:p.Leu69=
ENST00000261652.6:c.207C>A	ENSP00000261652.2:p.Leu69=
ENST00000579315.5:c.207C>A	ENSP00000464069.1:p.Leu69=
ENST00000581616.2:n.210C>A
ENST00000582931.5:n.111C>A
ENST00000583789.1:c.69C>A	ENSP00000462952.1:p.Leu23=
ENST00000584950.5:c.69C>A	ENSP00000463582.1:p.Leu23=
NM_012452.2:c.207C>A , LRG_120t1:c.207C>A	NP_036584.1:p.Leu69=
NM_012452.3:c.207C>A MANE Select	NP_036584.1:p.Leu69=