Canonical Allele Identifier: CA726572931

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs1375567715
• gnomAD v3: 17-16941858-A-T
• gnomAD v4: 17-16941858-A-T
• MyVariant Identifiers: chr17:g.16845172A>T (hg19) ; chr17:g.16941858A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941858A>T , CM000679.2:g.16941858A>T	GRCh38
NC_000017.10:g.16845172A>T , CM000679.1:g.16845172A>T	GRCh37
NC_000017.9:g.16785897A>T	NCBI36
NG_007281.1:g.35231T>A , LRG_120:g.35231T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.446-1347T>A MANE Select	ENSP00000261652.2:n.446-1347T>A
ENST00000261652.6:c.446-1347T>A	ENSP00000261652.2:n.446-1347T>A
ENST00000579315.5:c.445+6880T>A	ENSP00000464069.1:n.445+6880T>A
ENST00000581616.2:n.449-381T>A
ENST00000582931.5:n.349+6880T>A
ENST00000583789.1:c.308-1347T>A	ENSP00000462952.1:n.308-1347T>A
ENST00000584950.5:c.308-1347T>A	ENSP00000463582.1:n.308-1347T>A
NM_012452.2:c.446-1347T>A , LRG_120t1:c.446-1347T>A	NP_036584.1:n.446-1347T>A
NM_012452.3:c.446-1347T>A MANE Select	NP_036584.1:n.446-1347T>A