Canonical Allele Identifier: CA2250292636
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs2087510548

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941594A>G , CM000679.2:g.16941594A>G GRCh38
NC_000017.10:g.16844908A>G , CM000679.1:g.16844908A>G GRCh37
NC_000017.9:g.16785633A>G NCBI36
NG_007281.1:g.35495T>C , LRG_120:g.35495T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1083T>C MANE Select ENSP00000261652.2:n.446-1083T>C
ENST00000261652.6:c.446-1083T>C ENSP00000261652.2:n.446-1083T>C
ENST00000579315.5:c.445+7144T>C ENSP00000464069.1:n.445+7144T>C
ENST00000581616.2:n.449-117T>C
ENST00000582931.5:n.349+7144T>C
ENST00000583789.1:c.308-1083T>C ENSP00000462952.1:n.308-1083T>C
ENST00000584950.5:c.308-1083T>C ENSP00000463582.1:n.308-1083T>C
NM_012452.2:c.446-1083T>C , LRG_120t1:c.446-1083T>C NP_036584.1:n.446-1083T>C
NM_012452.3:c.446-1083T>C MANE Select NP_036584.1:n.446-1083T>C