Canonical Allele Identifier: CA13830181
Gene: TNFSF11 HGNC NCBI
COSMIC:
COSN16888175 (not active)
COSN20504460 (not active)
MyVariant.info:
GRCh38 chr13:g.42581032G>A
GRCh37 chr13:g.43155168G>A
gnomAD v2:
13:43155168 G / A
gnomAD v3:
13:42581032 G / A
gnomAD v4:
chr13-42581032-G-A
Joint Max Group AF 0.87881291 (SAS)
Genomes Max Group AF 0.85998366 (SAS)
Exomes Max Group AF 0.87877752 (SAS)
ClinVar RCV:
RCV001541578
ClinVar Variation:
1183681
dbSNP:
2277438
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42581032G>A , CM000675.2:g.42581032G>A GRCh38
NC_000013.10:g.43155168G>A , CM000675.1:g.43155168G>A GRCh37
NC_000013.9:g.42053168G>A NCBI36
NG_008990.1:g.23297G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398795.7:c.220-94G>A MANE Select ENSP00000381775.3:n.220-94G>A
ENST00000239849.8:c.79-94G>A ENSP00000239849.7:n.79-94G>A
ENST00000358545.6:c.1-94G>A ENSP00000351347.2:n.1-94G>A
ENST00000398795.6:c.220-94G>A ENSP00000381775.3:n.220-94G>A
ENST00000405262.6:c.1-94G>A ENSP00000384042.2:n.1-94G>A
ENST00000544862.5:c.1-94G>A ENSP00000444913.1:n.1-94G>A
NM_003701.3:c.220-94G>A NP_003692.1:n.220-94G>A
NM_033012.3:c.1-94G>A NP_143026.1:n.1-94G>A
XM_011535280.1:c.1-94G>A XP_011533582.1:n.1-94G>A
XM_011535280.2:c.1-94G>A XP_011533582.1:n.1-94G>A
XM_017020802.1:c.58-94G>A XP_016876291.1:n.58-94G>A
XM_017020803.2:c.1-94G>A XP_016876292.1:n.1-94G>A
NM_003701.4:c.220-94G>A MANE Select NP_003692.1:n.220-94G>A
NM_033012.4:c.1-94G>A NP_143026.1:n.1-94G>A
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