Canonical Allele Identifier: CA398520259

Gene: TNFRSF13B

Linked Data

• ClinVar Variation Id: 2291613
• ClinVar RCV Id: RCV002864599
• dbSNP Id: rs886052653
• gnomAD v4: 17-16948982-C-A
• MyVariant Identifiers: chr17:g.16852296C>A (hg19) ; chr17:g.16948982C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948982C>A , CM000679.2:g.16948982C>A	GRCh38
NC_000017.10:g.16852296C>A , CM000679.1:g.16852296C>A	GRCh37
NC_000017.9:g.16793021C>A	NCBI36
NG_007281.1:g.28107G>T , LRG_120:g.28107G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.201G>T MANE Select	ENSP00000261652.2:p.Arg67Ser
ENST00000261652.6:c.201G>T	ENSP00000261652.2:p.Arg67Ser
ENST00000579315.5:c.201G>T	ENSP00000464069.1:p.Arg67Ser
ENST00000581616.2:n.204G>T
ENST00000582931.5:n.105G>T
ENST00000583789.1:c.63G>T	ENSP00000462952.1:p.Trp21Cys
ENST00000584950.5:c.63G>T	ENSP00000463582.1:p.Trp21Cys
NM_012452.2:c.201G>T , LRG_120t1:c.201G>T	NP_036584.1:p.Arg67Ser
NM_012452.3:c.201G>T MANE Select	NP_036584.1:p.Arg67Ser