Canonical Allele Identifier: CA398520102
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948911G>T , CM000679.2:g.16948911G>T GRCh38
NC_000017.10:g.16852225G>T , CM000679.1:g.16852225G>T GRCh37
NC_000017.9:g.16792950G>T NCBI36
NG_007281.1:g.28178C>A , LRG_120:g.28178C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.272C>A MANE Select ENSP00000261652.2:p.Ser91Tyr
ENST00000261652.6:c.272C>A ENSP00000261652.2:p.Ser91Tyr
ENST00000579315.5:c.272C>A ENSP00000464069.1:p.Ser91Tyr
ENST00000581616.2:n.275C>A
ENST00000582931.5:n.176C>A
ENST00000583789.1:c.134C>A ENSP00000462952.1:p.Ser45Tyr
ENST00000584950.5:c.134C>A ENSP00000463582.1:p.Ser45Tyr
NM_012452.2:c.272C>A , LRG_120t1:c.272C>A NP_036584.1:p.Ser91Tyr
NM_012452.3:c.272C>A MANE Select NP_036584.1:p.Ser91Tyr