Canonical Allele Identifier: CA2250292581
Gene: TNFRSF13B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941562G= , CM000679.2:g.16941562G= GRCh38
NC_000017.10:g.16844876G= , CM000679.1:g.16844876G= GRCh37
NC_000017.9:g.16785601G= NCBI36
NG_007281.1:g.35527C= , LRG_120:g.35527C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1051C= MANE Select ENSP00000261652.2:n.446-1051C=
ENST00000261652.6:c.446-1051C= ENSP00000261652.2:n.446-1051C=
ENST00000579315.5:c.445+7176C= ENSP00000464069.1:n.445+7176C=
ENST00000581616.2:n.449-85C=
ENST00000582931.5:n.349+7176C=
ENST00000583789.1:c.308-1051C= ENSP00000462952.1:n.308-1051C=
ENST00000584950.5:c.308-1051C= ENSP00000463582.1:n.308-1051C=
NM_012452.2:c.446-1051C= , LRG_120t1:c.446-1051C= NP_036584.1:n.446-1051C=
NM_012452.3:c.446-1051C= MANE Select NP_036584.1:n.446-1051C=
Search 100 bp 5'
Search 100 bp 3'