Canonical Allele Identifier: CA288287762

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs565309002
• gnomAD v2: 17-16851895-GT-G
• gnomAD v3: 17-16948581-GT-G
• gnomAD v4: 17-16948581-GT-G
• MyVariant Identifiers: chr17:g.16851896del (hg19) ; chr17:g.16948582del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948589del , CM000679.2:g.16948589del	GRCh38
NC_000017.10:g.16851903del , CM000679.1:g.16851903del	GRCh37
NC_000017.9:g.16792628del	NCBI36
NG_007281.1:g.28507del , LRG_120:g.28507del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.445+156del MANE Select	ENSP00000261652.2:n.445+156del
ENST00000261652.6:c.445+156del	ENSP00000261652.2:n.445+156del
ENST00000579315.5:c.445+156del	ENSP00000464069.1:n.445+156del
ENST00000581616.2:n.448+156del
ENST00000582931.5:n.349+156del
ENST00000583789.1:c.307+156del	ENSP00000462952.1:n.307+156del
ENST00000584950.5:c.307+156del	ENSP00000463582.1:n.307+156del
NM_012452.2:c.445+156del , LRG_120t1:c.445+156del	NP_036584.1:n.445+156del
NM_012452.3:c.445+156del MANE Select	NP_036584.1:n.445+156del