Canonical Allele Identifier: CA398520169
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948942G>A , CM000679.2:g.16948942G>A GRCh38
NC_000017.10:g.16852256G>A , CM000679.1:g.16852256G>A GRCh37
NC_000017.9:g.16792981G>A NCBI36
NG_007281.1:g.28147C>T , LRG_120:g.28147C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.241C>T MANE Select ENSP00000261652.2:p.His81Tyr
ENST00000261652.6:c.241C>T ENSP00000261652.2:p.His81Tyr
ENST00000579315.5:c.241C>T ENSP00000464069.1:p.His81Tyr
ENST00000581616.2:n.244C>T
ENST00000582931.5:n.145C>T
ENST00000583789.1:c.103C>T ENSP00000462952.1:p.His35Tyr
ENST00000584950.5:c.103C>T ENSP00000463582.1:p.His35Tyr
NM_012452.2:c.241C>T , LRG_120t1:c.241C>T NP_036584.1:p.His81Tyr
NM_012452.3:c.241C>T MANE Select NP_036584.1:p.His81Tyr