Canonical Allele Identifier: CA398520242
Gene: TNFRSF13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.16852288C>G (hg19) chr17:g.16948974C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948974C>G , CM000679.2:g.16948974C>G GRCh38
NC_000017.10:g.16852288C>G , CM000679.1:g.16852288C>G GRCh37
NC_000017.9:g.16793013C>G NCBI36
NG_007281.1:g.28115G>C , LRG_120:g.28115G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.209G>C MANE Select ENSP00000261652.2:p.Ser70Thr
ENST00000261652.6:c.209G>C ENSP00000261652.2:p.Ser70Thr
ENST00000579315.5:c.209G>C ENSP00000464069.1:p.Ser70Thr
ENST00000581616.2:n.212G>C
ENST00000582931.5:n.113G>C
ENST00000583789.1:c.71G>C ENSP00000462952.1:p.Ser24Thr
ENST00000584950.5:c.71G>C ENSP00000463582.1:p.Ser24Thr
NM_012452.2:c.209G>C , LRG_120t1:c.209G>C NP_036584.1:p.Ser70Thr
NM_012452.3:c.209G>C MANE Select NP_036584.1:p.Ser70Thr
Search 100 bp 5'
Search 100 bp 3'