Canonical Allele Identifier: CA288283795

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs141019076
• gnomAD v2: 17-16844855-G-A
• gnomAD v3: 17-16941541-G-A
• gnomAD v4: 17-16941541-G-A
• MyVariant Identifiers: chr17:g.16844855G>A (hg19) ; chr17:g.16941541G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941541G>A , CM000679.2:g.16941541G>A	GRCh38
NC_000017.10:g.16844855G>A , CM000679.1:g.16844855G>A	GRCh37
NC_000017.9:g.16785580G>A	NCBI36
NG_007281.1:g.35548C>T , LRG_120:g.35548C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1030C>T MANE Select	ENSP00000261652.2:n.446-1030C>T
ENST00000261652.6:c.446-1030C>T	ENSP00000261652.2:n.446-1030C>T
ENST00000579315.5:c.445+7197C>T	ENSP00000464069.1:n.445+7197C>T
ENST00000581616.2:n.449-64C>T
ENST00000582931.5:n.349+7197C>T
ENST00000583789.1:c.308-1030C>T	ENSP00000462952.1:n.308-1030C>T
ENST00000584950.5:c.308-1030C>T	ENSP00000463582.1:n.308-1030C>T
NM_012452.2:c.446-1030C>T , LRG_120t1:c.446-1030C>T	NP_036584.1:n.446-1030C>T
NM_012452.3:c.446-1030C>T MANE Select	NP_036584.1:n.446-1030C>T