Canonical Allele Identifier: CA398520078
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948899T>C , CM000679.2:g.16948899T>C GRCh38
NC_000017.10:g.16852213T>C , CM000679.1:g.16852213T>C GRCh37
NC_000017.9:g.16792938T>C NCBI36
NG_007281.1:g.28190A>G , LRG_120:g.28190A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.284A>G MANE Select ENSP00000261652.2:p.Gln95Arg
ENST00000261652.6:c.284A>G ENSP00000261652.2:p.Gln95Arg
ENST00000579315.5:c.284A>G ENSP00000464069.1:p.Gln95Arg
ENST00000581616.2:n.287A>G
ENST00000582931.5:n.188A>G
ENST00000583789.1:c.146A>G ENSP00000462952.1:p.Gln49Arg
ENST00000584950.5:c.146A>G ENSP00000463582.1:p.Gln49Arg
NM_012452.2:c.284A>G , LRG_120t1:c.284A>G NP_036584.1:p.Gln95Arg
NM_012452.3:c.284A>G MANE Select NP_036584.1:p.Gln95Arg