Canonical Allele Identifier: CA14418274

Gene: TNFRSF13B

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16945825A>G , CM000679.2:g.16945825A>G	GRCh38
NC_000017.10:g.16849139A>G , CM000679.1:g.16849139A>G	GRCh37
NC_000017.9:g.16789864A>G	NCBI36
NG_007281.1:g.31264T>C , LRG_120:g.31264T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.445+2913T>C MANE Select	ENSP00000261652.2:n.445+2913T>C
ENST00000261652.6:c.445+2913T>C	ENSP00000261652.2:n.445+2913T>C
ENST00000579315.5:c.445+2913T>C	ENSP00000464069.1:n.445+2913T>C
ENST00000581616.2:n.448+2913T>C
ENST00000582931.5:n.349+2913T>C
ENST00000583789.1:c.307+2913T>C	ENSP00000462952.1:n.307+2913T>C
ENST00000584950.5:c.307+2913T>C	ENSP00000463582.1:n.307+2913T>C
NM_012452.2:c.445+2913T>C , LRG_120t1:c.445+2913T>C	NP_036584.1:n.445+2913T>C
NM_012452.3:c.445+2913T>C MANE Select	NP_036584.1:n.445+2913T>C