Canonical Allele Identifier: CA398520093
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948906A>G , CM000679.2:g.16948906A>G GRCh38
NC_000017.10:g.16852220A>G , CM000679.1:g.16852220A>G GRCh37
NC_000017.9:g.16792945A>G NCBI36
NG_007281.1:g.28183T>C , LRG_120:g.28183T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.277T>C MANE Select ENSP00000261652.2:p.Cys93Arg
ENST00000261652.6:c.277T>C ENSP00000261652.2:p.Cys93Arg
ENST00000579315.5:c.277T>C ENSP00000464069.1:p.Cys93Arg
ENST00000581616.2:n.280T>C
ENST00000582931.5:n.181T>C
ENST00000583789.1:c.139T>C ENSP00000462952.1:p.Cys47Arg
ENST00000584950.5:c.139T>C ENSP00000463582.1:p.Cys47Arg
NM_012452.2:c.277T>C , LRG_120t1:c.277T>C NP_036584.1:p.Cys93Arg
NM_012452.3:c.277T>C MANE Select NP_036584.1:p.Cys93Arg