Canonical Allele Identifier: CA498420335

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs1167588510
• gnomAD v2: 17-16852275-C-T
• gnomAD v4: 17-16948961-C-T
• MyVariant Identifiers: chr17:g.16852275C>T (hg19) ; chr17:g.16948961C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948961C>T , CM000679.2:g.16948961C>T	GRCh38
NC_000017.10:g.16852275C>T , CM000679.1:g.16852275C>T	GRCh37
NC_000017.9:g.16793000C>T	NCBI36
NG_007281.1:g.28128G>A , LRG_120:g.28128G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.222G>A MANE Select	ENSP00000261652.2:p.Glu74=
ENST00000261652.6:c.222G>A	ENSP00000261652.2:p.Glu74=
ENST00000579315.5:c.222G>A	ENSP00000464069.1:p.Glu74=
ENST00000581616.2:n.225G>A
ENST00000582931.5:n.126G>A
ENST00000583789.1:c.84G>A	ENSP00000462952.1:p.Glu28=
ENST00000584950.5:c.84G>A	ENSP00000463582.1:p.Glu28=
NM_012452.2:c.222G>A , LRG_120t1:c.222G>A	NP_036584.1:p.Glu74=
NM_012452.3:c.222G>A MANE Select	NP_036584.1:p.Glu74=