Canonical Allele Identifier: CA398520113
Gene: TNFRSF13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.16852230A>T (hg19) chr17:g.16948916A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948916A>T , CM000679.2:g.16948916A>T GRCh38
NC_000017.10:g.16852230A>T , CM000679.1:g.16852230A>T GRCh37
NC_000017.9:g.16792955A>T NCBI36
NG_007281.1:g.28173T>A , LRG_120:g.28173T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.267T>A MANE Select ENSP00000261652.2:p.Cys89Ter
ENST00000261652.6:c.267T>A ENSP00000261652.2:p.Cys89Ter
ENST00000579315.5:c.267T>A ENSP00000464069.1:p.Cys89Ter
ENST00000581616.2:n.270T>A
ENST00000582931.5:n.171T>A
ENST00000583789.1:c.129T>A ENSP00000462952.1:p.Cys43Ter
ENST00000584950.5:c.129T>A ENSP00000463582.1:p.Cys43Ter
NM_012452.2:c.267T>A , LRG_120t1:c.267T>A NP_036584.1:p.Cys89Ter
NM_012452.3:c.267T>A MANE Select NP_036584.1:p.Cys89Ter
Search 100 bp 5'
Search 100 bp 3'