Canonical Allele Identifier: CA2250292631
Gene: TNFRSF13B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941592A= , CM000679.2:g.16941592A= GRCh38
NC_000017.10:g.16844906A= , CM000679.1:g.16844906A= GRCh37
NC_000017.9:g.16785631A= NCBI36
NG_007281.1:g.35497T= , LRG_120:g.35497T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1081T= MANE Select ENSP00000261652.2:n.446-1081T=
ENST00000261652.6:c.446-1081T= ENSP00000261652.2:n.446-1081T=
ENST00000579315.5:c.445+7146T= ENSP00000464069.1:n.445+7146T=
ENST00000581616.2:n.449-115T=
ENST00000582931.5:n.349+7146T=
ENST00000583789.1:c.308-1081T= ENSP00000462952.1:n.308-1081T=
ENST00000584950.5:c.308-1081T= ENSP00000463582.1:n.308-1081T=
NM_012452.2:c.446-1081T= , LRG_120t1:c.446-1081T= NP_036584.1:n.446-1081T=
NM_012452.3:c.446-1081T= MANE Select NP_036584.1:n.446-1081T=
Search 100 bp 5'
Search 100 bp 3'