Canonical Allele Identifier: CA398520230
Gene: TNFRSF13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.16852283G>T (hg19) chr17:g.16948969G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948969G>T , CM000679.2:g.16948969G>T GRCh38
NC_000017.10:g.16852283G>T , CM000679.1:g.16852283G>T GRCh37
NC_000017.9:g.16793008G>T NCBI36
NG_007281.1:g.28120C>A , LRG_120:g.28120C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.214C>A MANE Select ENSP00000261652.2:p.Arg72Ser
ENST00000261652.6:c.214C>A ENSP00000261652.2:p.Arg72Ser
ENST00000579315.5:c.214C>A ENSP00000464069.1:p.Arg72Ser
ENST00000581616.2:n.217C>A
ENST00000582931.5:n.118C>A
ENST00000583789.1:c.76C>A ENSP00000462952.1:p.Arg26Ser
ENST00000584950.5:c.76C>A ENSP00000463582.1:p.Arg26Ser
NM_012452.2:c.214C>A , LRG_120t1:c.214C>A NP_036584.1:p.Arg72Ser
NM_012452.3:c.214C>A MANE Select NP_036584.1:p.Arg72Ser
Search 100 bp 5'
Search 100 bp 3'