Canonical Allele Identifier: CA398520132
Gene: TNFRSF13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.16852239G>C (hg19) chr17:g.16948925G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948925G>C , CM000679.2:g.16948925G>C GRCh38
NC_000017.10:g.16852239G>C , CM000679.1:g.16852239G>C GRCh37
NC_000017.9:g.16792964G>C NCBI36
NG_007281.1:g.28164C>G , LRG_120:g.28164C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.258C>G MANE Select ENSP00000261652.2:p.Cys86Trp
ENST00000261652.6:c.258C>G ENSP00000261652.2:p.Cys86Trp
ENST00000579315.5:c.258C>G ENSP00000464069.1:p.Cys86Trp
ENST00000581616.2:n.261C>G
ENST00000582931.5:n.162C>G
ENST00000583789.1:c.120C>G ENSP00000462952.1:p.Cys40Trp
ENST00000584950.5:c.120C>G ENSP00000463582.1:p.Cys40Trp
NM_012452.2:c.258C>G , LRG_120t1:c.258C>G NP_036584.1:p.Cys86Trp
NM_012452.3:c.258C>G MANE Select NP_036584.1:p.Cys86Trp
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