Canonical Allele Identifier: CA8414053
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1056901
ClinVar RCV Id: RCV001365796 RCV002476669
dbSNP Id: rs549493928
ExAC: 17:16852214 G / C
gnomAD v2: 17-16852214-G-C
gnomAD v3: 17-16948900-G-C
gnomAD v4: 17-16948900-G-C
MyVariant Identifiers: chr17:g.16852214G>C (hg19) chr17:g.16948900G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948900G>C , CM000679.2:g.16948900G>C GRCh38
NC_000017.10:g.16852214G>C , CM000679.1:g.16852214G>C GRCh37
NC_000017.9:g.16792939G>C NCBI36
NG_007281.1:g.28189C>G , LRG_120:g.28189C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.283C>G MANE Select ENSP00000261652.2:p.Gln95Glu
ENST00000261652.6:c.283C>G ENSP00000261652.2:p.Gln95Glu
ENST00000579315.5:c.283C>G ENSP00000464069.1:p.Gln95Glu
ENST00000581616.2:n.286C>G
ENST00000582931.5:n.187C>G
ENST00000583789.1:c.145C>G ENSP00000462952.1:p.Gln49Glu
ENST00000584950.5:c.145C>G ENSP00000463582.1:p.Gln49Glu
NM_012452.2:c.283C>G , LRG_120t1:c.283C>G NP_036584.1:p.Gln95Glu
NM_012452.3:c.283C>G MANE Select NP_036584.1:p.Gln95Glu
Search 100 bp 5'
Search 100 bp 3'