Canonical Allele Identifier: CA2636331892

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16972038-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16972038_16972039insG , CM000679.2:g.16972038_16972039insG	GRCh38
NC_000017.10:g.16875352_16875353insG , CM000679.1:g.16875352_16875353insG	GRCh37
NC_000017.9:g.16816077_16816078insG	NCBI36
NG_007281.1:g.5050_5051insC , LRG_120:g.5050_5051insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.37_38insC MANE Select	ENSP00000261652.2:p.Ser13ThrfsTer?
ENST00000261652.6:c.37_38insC	ENSP00000261652.2:p.Ser13ThrfsTer?
ENST00000579315.5:c.37_38insC	ENSP00000464069.1:p.Ser13ThrfsTer?
ENST00000581616.2:n.40_41insC
ENST00000582931.5:n.79_80insC
ENST00000583789.1:c.37_38insC	ENSP00000462952.1:p.Ser13ThrfsTer22
ENST00000584950.5:c.37_38insC	ENSP00000463582.1:p.Ser13ThrfsTer22
NM_012452.2:c.37_38insC , LRG_120t1:c.37_38insC	NP_036584.1:p.Ser13ThrfsTer?
NM_012452.3:c.37_38insC MANE Select	NP_036584.1:p.Ser13ThrfsTer?