Canonical Allele Identifier: CA2636330265

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16949057-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16949058_16949059del , CM000679.2:g.16949058_16949059del	GRCh38
NC_000017.10:g.16852372_16852373del , CM000679.1:g.16852372_16852373del	GRCh37
NC_000017.9:g.16793097_16793098del	NCBI36
NG_007281.1:g.28030_28031del , LRG_120:g.28030_28031del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.200-76_200-75del MANE Select	ENSP00000261652.2:n.200-76_200-75del
ENST00000261652.6:c.200-76_200-75del	ENSP00000261652.2:n.200-76_200-75del
ENST00000579315.5:c.200-76_200-75del	ENSP00000464069.1:n.200-76_200-75del
ENST00000581616.2:n.203-76_203-75del
ENST00000582931.5:n.104-76_104-75del
ENST00000583789.1:c.62-76_62-75del	ENSP00000462952.1:n.62-76_62-75del
ENST00000584950.5:c.62-76_62-75del	ENSP00000463582.1:n.62-76_62-75del
NM_012452.2:c.200-76_200-75del , LRG_120t1:c.200-76_200-75del	NP_036584.1:n.200-76_200-75del
NM_012452.3:c.200-76_200-75del MANE Select	NP_036584.1:n.200-76_200-75del