Canonical Allele Identifier: CA398520023
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1910910
ClinVar RCV Id: RCV002589466
dbSNP Id: rs1201043139

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948874G>C , CM000679.2:g.16948874G>C GRCh38
NC_000017.10:g.16852188G>C , CM000679.1:g.16852188G>C GRCh37
NC_000017.9:g.16792913G>C NCBI36
NG_007281.1:g.28215C>G , LRG_120:g.28215C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261652.7:c.309C>G MANE Select ENSP00000261652.2:p.Phe103Leu
ENST00000261652.6:c.309C>G ENSP00000261652.2:p.Phe103Leu
ENST00000579315.5:c.309C>G ENSP00000464069.1:p.Phe103Leu
ENST00000581616.2:n.312C>G
ENST00000582931.5:n.213C>G
ENST00000583789.1:c.171C>G ENSP00000462952.1:p.Phe57Leu
ENST00000584950.5:c.171C>G ENSP00000463582.1:p.Phe57Leu
NM_012452.2:c.309C>G , LRG_120t1:c.309C>G NP_036584.1:p.Phe103Leu
NM_012452.3:c.309C>G MANE Select NP_036584.1:p.Phe103Leu