Canonical Allele Identifier: CA8414064
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 733838
ClinVar RCV Id: RCV000909193
dbSNP Id: rs146436713
ExAC: 17:16852271 C / T
gnomAD v2: 17-16852271-C-T
gnomAD v3: 17-16948957-C-T
gnomAD v4: 17-16948957-C-T
COSMIC: COSM1582333
MyVariant Identifiers: chr17:g.16852271C>T (hg19) chr17:g.16948957C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948957C>T , CM000679.2:g.16948957C>T GRCh38
NC_000017.10:g.16852271C>T , CM000679.1:g.16852271C>T GRCh37
NC_000017.9:g.16792996C>T NCBI36
NG_007281.1:g.28132G>A , LRG_120:g.28132G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.226G>A MANE Select ENSP00000261652.2:p.Gly76Ser
ENST00000261652.6:c.226G>A ENSP00000261652.2:p.Gly76Ser
ENST00000579315.5:c.226G>A ENSP00000464069.1:p.Gly76Ser
ENST00000581616.2:n.229G>A
ENST00000582931.5:n.130G>A
ENST00000583789.1:c.88G>A ENSP00000462952.1:p.Gly30Ser
ENST00000584950.5:c.88G>A ENSP00000463582.1:p.Gly30Ser
NM_012452.2:c.226G>A , LRG_120t1:c.226G>A NP_036584.1:p.Gly76Ser
NM_012452.3:c.226G>A MANE Select NP_036584.1:p.Gly76Ser
Search 100 bp 5'
Search 100 bp 3'