Canonical Allele Identifier: CA2733498573

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs2143644640

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941771C>G , CM000679.2:g.16941771C>G	GRCh38
NC_000017.10:g.16845085C>G , CM000679.1:g.16845085C>G	GRCh37
NC_000017.9:g.16785810C>G	NCBI36
NG_007281.1:g.35318G>C , LRG_120:g.35318G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1260G>C MANE Select	ENSP00000261652.2:n.446-1260G>C
ENST00000261652.6:c.446-1260G>C	ENSP00000261652.2:n.446-1260G>C
ENST00000579315.5:c.445+6967G>C	ENSP00000464069.1:n.445+6967G>C
ENST00000581616.2:n.449-294G>C
ENST00000582931.5:n.349+6967G>C
ENST00000583789.1:c.308-1260G>C	ENSP00000462952.1:n.308-1260G>C
ENST00000584950.5:c.308-1260G>C	ENSP00000463582.1:n.308-1260G>C
NM_012452.2:c.446-1260G>C , LRG_120t1:c.446-1260G>C	NP_036584.1:n.446-1260G>C
NM_012452.3:c.446-1260G>C MANE Select	NP_036584.1:n.446-1260G>C