Canonical Allele Identifier: CA398520179
Gene: TNFRSF13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.16852260A>T (hg19) chr17:g.16948946A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948946A>T , CM000679.2:g.16948946A>T GRCh38
NC_000017.10:g.16852260A>T , CM000679.1:g.16852260A>T GRCh37
NC_000017.9:g.16792985A>T NCBI36
NG_007281.1:g.28143T>A , LRG_120:g.28143T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.237T>A MANE Select ENSP00000261652.2:p.Tyr79Ter
ENST00000261652.6:c.237T>A ENSP00000261652.2:p.Tyr79Ter
ENST00000579315.5:c.237T>A ENSP00000464069.1:p.Tyr79Ter
ENST00000581616.2:n.240T>A
ENST00000582931.5:n.141T>A
ENST00000583789.1:c.99T>A ENSP00000462952.1:p.Tyr33Ter
ENST00000584950.5:c.99T>A ENSP00000463582.1:p.Tyr33Ter
NM_012452.2:c.237T>A , LRG_120t1:c.237T>A NP_036584.1:p.Tyr79Ter
NM_012452.3:c.237T>A MANE Select NP_036584.1:p.Tyr79Ter
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