Canonical Allele Identifier: CA2636330284

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16949062-AGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16949063_16949065del , CM000679.2:g.16949063_16949065del	GRCh38
NC_000017.10:g.16852377_16852379del , CM000679.1:g.16852377_16852379del	GRCh37
NC_000017.9:g.16793102_16793104del	NCBI36
NG_007281.1:g.28024_28026del , LRG_120:g.28024_28026del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.200-82_200-80del MANE Select	ENSP00000261652.2:n.200-82_200-80del
ENST00000261652.6:c.200-82_200-80del	ENSP00000261652.2:n.200-82_200-80del
ENST00000579315.5:c.200-82_200-80del	ENSP00000464069.1:n.200-82_200-80del
ENST00000581616.2:n.203-82_203-80del
ENST00000582931.5:n.104-82_104-80del
ENST00000583789.1:c.62-82_62-80del	ENSP00000462952.1:n.62-82_62-80del
ENST00000584950.5:c.62-82_62-80del	ENSP00000463582.1:n.62-82_62-80del
NM_012452.2:c.200-82_200-80del , LRG_120t1:c.200-82_200-80del	NP_036584.1:n.200-82_200-80del
NM_012452.3:c.200-82_200-80del MANE Select	NP_036584.1:n.200-82_200-80del