Canonical Allele Identifier: CA5206977
Gene: TNFSF15 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.114790969T>C
GRCh37 chr9:g.117553249T>C
Revel Score:
ENST00000374044 0.000
gnomAD v2:
9:117553249 T / C
gnomAD v3:
9:114790969 T / C
gnomAD v4:
chr9-114790969-T-C
Joint Max Group AF 0.92646443 (AFR)
Genomes Max Group AF 0.92082121 (AFR)
Exomes Max Group AF 0.92833818 (AFR)
dbSNP:
4246905
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114790969T>C , CM000671.2:g.114790969T>C GRCh38
NC_000009.11:g.117553249T>C , CM000671.1:g.117553249T>C GRCh37
NC_000009.10:g.116593070T>C NCBI36
NG_011488.2:g.20160A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.302-63A>G MANE Select ENSP00000363157.3:n.302-63A>G
ENST00000374044.1:c.8A>G ENSP00000363156.1:p.His3Arg
ENST00000374045.4:c.302-63A>G ENSP00000363157.3:n.302-63A>G
NM_001204344.1:c.125-63A>G NP_001191273.1:n.125-63A>G
NM_005118.3:c.302-63A>G NP_005109.2:n.302-63A>G
NM_005118.4:c.302-63A>G MANE Select NP_005109.2:n.302-63A>G
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