Canonical Allele Identifier: CA2250292694
Gene: TNFRSF13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941631C= , CM000679.2:g.16941631C= GRCh38
NC_000017.10:g.16844945C= , CM000679.1:g.16844945C= GRCh37
NC_000017.9:g.16785670C= NCBI36
NG_007281.1:g.35458G= , LRG_120:g.35458G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1120G= MANE Select ENSP00000261652.2:n.446-1120G=
ENST00000261652.6:c.446-1120G= ENSP00000261652.2:n.446-1120G=
ENST00000579315.5:c.445+7107G= ENSP00000464069.1:n.445+7107G=
ENST00000581616.2:n.449-154G=
ENST00000582931.5:n.349+7107G=
ENST00000583789.1:c.308-1120G= ENSP00000462952.1:n.308-1120G=
ENST00000584950.5:c.308-1120G= ENSP00000463582.1:n.308-1120G=
NM_012452.2:c.446-1120G= , LRG_120t1:c.446-1120G= NP_036584.1:n.446-1120G=
NM_012452.3:c.446-1120G= MANE Select NP_036584.1:n.446-1120G=
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