Canonical Allele Identifier: CA398520151
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948933T>A , CM000679.2:g.16948933T>A GRCh38
NC_000017.10:g.16852247T>A , CM000679.1:g.16852247T>A GRCh37
NC_000017.9:g.16792972T>A NCBI36
NG_007281.1:g.28156A>T , LRG_120:g.28156A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.250A>T MANE Select ENSP00000261652.2:p.Arg84Trp
ENST00000261652.6:c.250A>T ENSP00000261652.2:p.Arg84Trp
ENST00000579315.5:c.250A>T ENSP00000464069.1:p.Arg84Trp
ENST00000581616.2:n.253A>T
ENST00000582931.5:n.154A>T
ENST00000583789.1:c.112A>T ENSP00000462952.1:p.Arg38Trp
ENST00000584950.5:c.112A>T ENSP00000463582.1:p.Arg38Trp
NM_012452.2:c.250A>T , LRG_120t1:c.250A>T NP_036584.1:p.Arg84Trp
NM_012452.3:c.250A>T MANE Select NP_036584.1:p.Arg84Trp