Canonical Allele Identifier: CA398520162
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948939G>C , CM000679.2:g.16948939G>C GRCh38
NC_000017.10:g.16852253G>C , CM000679.1:g.16852253G>C GRCh37
NC_000017.9:g.16792978G>C NCBI36
NG_007281.1:g.28150C>G , LRG_120:g.28150C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.244C>G MANE Select ENSP00000261652.2:p.Leu82Val
ENST00000261652.6:c.244C>G ENSP00000261652.2:p.Leu82Val
ENST00000579315.5:c.244C>G ENSP00000464069.1:p.Leu82Val
ENST00000581616.2:n.247C>G
ENST00000582931.5:n.148C>G
ENST00000583789.1:c.106C>G ENSP00000462952.1:p.Leu36Val
ENST00000584950.5:c.106C>G ENSP00000463582.1:p.Leu36Val
NM_012452.2:c.244C>G , LRG_120t1:c.244C>G NP_036584.1:p.Leu82Val
NM_012452.3:c.244C>G MANE Select NP_036584.1:p.Leu82Val