Canonical Allele Identifier: CA8414057
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 618436
ClinVar RCV Id: RCV000756794 RCV000800201 RCV001844233 RCV002508946
dbSNP Id: rs72553877
ExAC: 17:16852237 A / T
gnomAD v2: 17-16852237-A-T
gnomAD v3: 17-16948923-A-T
gnomAD v4: 17-16948923-A-T
MyVariant Identifiers: chr17:g.16852237A>T (hg19) chr17:g.16948923A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948923A>T , CM000679.2:g.16948923A>T GRCh38
NC_000017.10:g.16852237A>T , CM000679.1:g.16852237A>T GRCh37
NC_000017.9:g.16792962A>T NCBI36
NG_007281.1:g.28166T>A , LRG_120:g.28166T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.260T>A MANE Select ENSP00000261652.2:p.Ile87Asn
ENST00000261652.6:c.260T>A ENSP00000261652.2:p.Ile87Asn
ENST00000579315.5:c.260T>A ENSP00000464069.1:p.Ile87Asn
ENST00000581616.2:n.263T>A
ENST00000582931.5:n.164T>A
ENST00000583789.1:c.122T>A ENSP00000462952.1:p.Ile41Asn
ENST00000584950.5:c.122T>A ENSP00000463582.1:p.Ile41Asn
NM_012452.2:c.260T>A , LRG_120t1:c.260T>A NP_036584.1:p.Ile87Asn
NM_012452.3:c.260T>A MANE Select NP_036584.1:p.Ile87Asn
Search 100 bp 5'
Search 100 bp 3'