Canonical Allele Identifier: CA398520091
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948905C>T , CM000679.2:g.16948905C>T GRCh38
NC_000017.10:g.16852219C>T , CM000679.1:g.16852219C>T GRCh37
NC_000017.9:g.16792944C>T NCBI36
NG_007281.1:g.28184G>A , LRG_120:g.28184G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.278G>A MANE Select ENSP00000261652.2:p.Cys93Tyr
ENST00000261652.6:c.278G>A ENSP00000261652.2:p.Cys93Tyr
ENST00000579315.5:c.278G>A ENSP00000464069.1:p.Cys93Tyr
ENST00000581616.2:n.281G>A
ENST00000582931.5:n.182G>A
ENST00000583789.1:c.140G>A ENSP00000462952.1:p.Cys47Tyr
ENST00000584950.5:c.140G>A ENSP00000463582.1:p.Cys47Tyr
NM_012452.2:c.278G>A , LRG_120t1:c.278G>A NP_036584.1:p.Cys93Tyr
NM_012452.3:c.278G>A MANE Select NP_036584.1:p.Cys93Tyr