Canonical Allele Identifier: CA374686414
Gene: TNFSF15 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.114790814T>C
GRCh37 chr9:g.117553094T>C
Revel Score:
ENST00000374045 (MANE Select) 0.490
ENST00000374044 0.490
gnomAD v2:
9:117553094 T / C
gnomAD v3:
9:114790814 T / C
gnomAD v4:
chr9-114790814-T-C
Joint Max Group AF 0.00035939 (AMR)
Genomes Max Group AF 0.00097544 (AMR)
Exomes Max Group AF 0.00008861 (AMR)
ClinVar Allele:
2261454
ClinVar RCV:
RCV004130077
ClinVar Variation:
2272923
dbSNP:
1403226813
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114790814T>C , CM000671.2:g.114790814T>C GRCh38
NC_000009.11:g.117553094T>C , CM000671.1:g.117553094T>C GRCh37
NC_000009.10:g.116592915T>C NCBI36
NG_011488.2:g.20315A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.394A>G MANE Select ENSP00000363157.3:p.Met132Val
ENST00000374044.1:c.163A>G ENSP00000363156.1:p.Met55Val
ENST00000374045.4:c.394A>G ENSP00000363157.3:p.Met132Val
NM_001204344.1:c.217A>G NP_001191273.1:p.Met73Val
NM_005118.3:c.394A>G NP_005109.2:p.Met132Val
NM_005118.4:c.394A>G MANE Select NP_005109.2:p.Met132Val
Search 100 bp 5'
Search 100 bp 3'