Canonical Allele Identifier: CA398520040

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs2087568342
• MyVariant Identifiers: chr17:g.16852196C>T (hg19) ; chr17:g.16948882C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948882C>T , CM000679.2:g.16948882C>T	GRCh38
NC_000017.10:g.16852196C>T , CM000679.1:g.16852196C>T	GRCh37
NC_000017.9:g.16792921C>T	NCBI36
NG_007281.1:g.28207G>A , LRG_120:g.28207G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.301G>A MANE Select	ENSP00000261652.2:p.Ala101Thr
ENST00000261652.6:c.301G>A	ENSP00000261652.2:p.Ala101Thr
ENST00000579315.5:c.301G>A	ENSP00000464069.1:p.Ala101Thr
ENST00000581616.2:n.304G>A
ENST00000582931.5:n.205G>A
ENST00000583789.1:c.163G>A	ENSP00000462952.1:p.Ala55Thr
ENST00000584950.5:c.163G>A	ENSP00000463582.1:p.Ala55Thr
NM_012452.2:c.301G>A , LRG_120t1:c.301G>A	NP_036584.1:p.Ala101Thr
NM_012452.3:c.301G>A MANE Select	NP_036584.1:p.Ala101Thr