Canonical Allele Identifier: CA8414060
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1465323
ClinVar RCV Id: RCV001990251
dbSNP Id: rs769360883
ExAC: 17:16852256 G / T
gnomAD v2: 17-16852256-G-T
gnomAD v3: 17-16948942-G-T
gnomAD v4: 17-16948942-G-T
MyVariant Identifiers: chr17:g.16852256G>T (hg19) chr17:g.16948942G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948942G>T , CM000679.2:g.16948942G>T GRCh38
NC_000017.10:g.16852256G>T , CM000679.1:g.16852256G>T GRCh37
NC_000017.9:g.16792981G>T NCBI36
NG_007281.1:g.28147C>A , LRG_120:g.28147C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.241C>A MANE Select ENSP00000261652.2:p.His81Asn
ENST00000261652.6:c.241C>A ENSP00000261652.2:p.His81Asn
ENST00000579315.5:c.241C>A ENSP00000464069.1:p.His81Asn
ENST00000581616.2:n.244C>A
ENST00000582931.5:n.145C>A
ENST00000583789.1:c.103C>A ENSP00000462952.1:p.His35Asn
ENST00000584950.5:c.103C>A ENSP00000463582.1:p.His35Asn
NM_012452.2:c.241C>A , LRG_120t1:c.241C>A NP_036584.1:p.His81Asn
NM_012452.3:c.241C>A MANE Select NP_036584.1:p.His81Asn
Search 100 bp 5'
Search 100 bp 3'