Canonical Allele Identifier: CA288288228
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs67234667

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16949076dup , CM000679.2:g.16949076dup GRCh38
NC_000017.10:g.16852390dup , CM000679.1:g.16852390dup GRCh37
NC_000017.9:g.16793115dup NCBI36
NG_007281.1:g.28023dup , LRG_120:g.28023dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.200-83dup MANE Select ENSP00000261652.2:n.200-83dup
ENST00000261652.6:c.200-83dup ENSP00000261652.2:n.200-83dup
ENST00000579315.5:c.200-83dup ENSP00000464069.1:n.200-83dup
ENST00000581616.2:n.203-83dup
ENST00000582931.5:n.104-83dup
ENST00000583789.1:c.62-83dup ENSP00000462952.1:n.62-83dup
ENST00000584950.5:c.62-83dup ENSP00000463582.1:n.62-83dup
NM_012452.2:c.200-83dup , LRG_120t1:c.200-83dup NP_036584.1:n.200-83dup
NM_012452.3:c.200-83dup MANE Select NP_036584.1:n.200-83dup