Canonical Allele Identifier: CA398519766

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852069C>A (hg19) ; chr17:g.16948755C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948755C>A , CM000679.2:g.16948755C>A	GRCh38
NC_000017.10:g.16852069C>A , CM000679.1:g.16852069C>A	GRCh37
NC_000017.9:g.16792794C>A	NCBI36
NG_007281.1:g.28334G>T , LRG_120:g.28334G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.428G>T MANE Select	ENSP00000261652.2:p.Gly143Val
ENST00000261652.6:c.428G>T	ENSP00000261652.2:p.Gly143Val
ENST00000579315.5:c.428G>T	ENSP00000464069.1:p.Gly143Val
ENST00000581616.2:n.431G>T
ENST00000582931.5:n.332G>T
ENST00000583789.1:c.290G>T	ENSP00000462952.1:p.Gly97Val
ENST00000584950.5:c.290G>T	ENSP00000463582.1:p.Gly97Val
NM_012452.2:c.428G>T , LRG_120t1:c.428G>T	NP_036584.1:p.Gly143Val
NM_012452.3:c.428G>T MANE Select	NP_036584.1:p.Gly143Val