Canonical Allele Identifier: CA498420318

Gene: TNFRSF13B

Linked Data

• ClinVar Variation Id: 2698596
• ClinVar RCV Id: RCV003505503
• MyVariant Identifiers: chr17:g.16852245C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948931C>T , CM000679.2:g.16948931C>T	GRCh38
NC_000017.10:g.16852245C>T , CM000679.1:g.16852245C>T	GRCh37
NC_000017.9:g.16792970C>T	NCBI36
NG_007281.1:g.28158G>A , LRG_120:g.28158G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.252G>A MANE Select	ENSP00000261652.2:p.Arg84=
ENST00000261652.6:c.252G>A	ENSP00000261652.2:p.Arg84=
ENST00000579315.5:c.252G>A	ENSP00000464069.1:p.Arg84=
ENST00000581616.2:n.255G>A
ENST00000582931.5:n.156G>A
ENST00000583789.1:c.114G>A	ENSP00000462952.1:p.Arg38=
ENST00000584950.5:c.114G>A	ENSP00000463582.1:p.Arg38=
NM_012452.2:c.252G>A , LRG_120t1:c.252G>A	NP_036584.1:p.Arg84=
NM_012452.3:c.252G>A MANE Select	NP_036584.1:p.Arg84=