Canonical Allele Identifier: CA398520125
Gene: TNFRSF13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.16852235T>G (hg19) chr17:g.16948921T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948921T>G , CM000679.2:g.16948921T>G GRCh38
NC_000017.10:g.16852235T>G , CM000679.1:g.16852235T>G GRCh37
NC_000017.9:g.16792960T>G NCBI36
NG_007281.1:g.28168A>C , LRG_120:g.28168A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.262A>C MANE Select ENSP00000261652.2:p.Ser88Arg
ENST00000261652.6:c.262A>C ENSP00000261652.2:p.Ser88Arg
ENST00000579315.5:c.262A>C ENSP00000464069.1:p.Ser88Arg
ENST00000581616.2:n.265A>C
ENST00000582931.5:n.166A>C
ENST00000583789.1:c.124A>C ENSP00000462952.1:p.Ser42Arg
ENST00000584950.5:c.124A>C ENSP00000463582.1:p.Ser42Arg
NM_012452.2:c.262A>C , LRG_120t1:c.262A>C NP_036584.1:p.Ser88Arg
NM_012452.3:c.262A>C MANE Select NP_036584.1:p.Ser88Arg
Search 100 bp 5'
Search 100 bp 3'