Canonical Allele Identifier: CA2636329164

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16948629-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948629G>T , CM000679.2:g.16948629G>T	GRCh38
NC_000017.10:g.16851943G>T , CM000679.1:g.16851943G>T	GRCh37
NC_000017.9:g.16792668G>T	NCBI36
NG_007281.1:g.28460C>A , LRG_120:g.28460C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.445+109C>A MANE Select	ENSP00000261652.2:n.445+109C>A
ENST00000261652.6:c.445+109C>A	ENSP00000261652.2:n.445+109C>A
ENST00000579315.5:c.445+109C>A	ENSP00000464069.1:n.445+109C>A
ENST00000581616.2:n.448+109C>A
ENST00000582931.5:n.349+109C>A
ENST00000583789.1:c.307+109C>A	ENSP00000462952.1:n.307+109C>A
ENST00000584950.5:c.307+109C>A	ENSP00000463582.1:n.307+109C>A
NM_012452.2:c.445+109C>A , LRG_120t1:c.445+109C>A	NP_036584.1:n.445+109C>A
NM_012452.3:c.445+109C>A MANE Select	NP_036584.1:n.445+109C>A