Canonical Allele Identifier: CA8414048
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs75885572

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948884C>T , CM000679.2:g.16948884C>T GRCh38
NC_000017.10:g.16852198C>T , CM000679.1:g.16852198C>T GRCh37
NC_000017.9:g.16792923C>T NCBI36
NG_007281.1:g.28205G>A , LRG_120:g.28205G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.299G>A MANE Select ENSP00000261652.2:p.Cys100Tyr
ENST00000261652.6:c.299G>A ENSP00000261652.2:p.Cys100Tyr
ENST00000579315.5:c.299G>A ENSP00000464069.1:p.Cys100Tyr
ENST00000581616.2:n.302G>A
ENST00000582931.5:n.203G>A
ENST00000583789.1:c.161G>A ENSP00000462952.1:p.Cys54Tyr
ENST00000584950.5:c.161G>A ENSP00000463582.1:p.Cys54Tyr
NM_012452.2:c.299G>A , LRG_120t1:c.299G>A NP_036584.1:p.Cys100Tyr
NM_012452.3:c.299G>A MANE Select NP_036584.1:p.Cys100Tyr