Canonical Allele Identifier: CA398520240
Gene: TNFRSF13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.16852287G>T (hg19) chr17:g.16948973G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948973G>T , CM000679.2:g.16948973G>T GRCh38
NC_000017.10:g.16852287G>T , CM000679.1:g.16852287G>T GRCh37
NC_000017.9:g.16793012G>T NCBI36
NG_007281.1:g.28116C>A , LRG_120:g.28116C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.210C>A MANE Select ENSP00000261652.2:p.Ser70Arg
ENST00000261652.6:c.210C>A ENSP00000261652.2:p.Ser70Arg
ENST00000579315.5:c.210C>A ENSP00000464069.1:p.Ser70Arg
ENST00000581616.2:n.213C>A
ENST00000582931.5:n.114C>A
ENST00000583789.1:c.72C>A ENSP00000462952.1:p.Ser24Arg
ENST00000584950.5:c.72C>A ENSP00000463582.1:p.Ser24Arg
NM_012452.2:c.210C>A , LRG_120t1:c.210C>A NP_036584.1:p.Ser70Arg
NM_012452.3:c.210C>A MANE Select NP_036584.1:p.Ser70Arg
Search 100 bp 5'
Search 100 bp 3'