Canonical Allele Identifier: CA15600991
Gene: TNFSF15 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.114785492T>C
GRCh37 chr9:g.117547772T>C
gnomAD v2:
9:117547772 T / C
gnomAD v3:
9:114785492 T / C
gnomAD v4:
chr9-114785492-T-C
Joint Max Group AF 0.88249416 (AFR)
Genomes Max Group AF 0.88249416 (AFR)
Exomes Max Group AF 0.32662601 (NFE)
ClinVar Allele:
1708937
ClinVar RCV:
RCV002291813
ClinVar Variation:
1710526
dbSNP:
10114470
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785492T>C , CM000671.2:g.114785492T>C GRCh38
NC_000009.11:g.117547772T>C , CM000671.1:g.117547772T>C GRCh37
NC_000009.10:g.116587593T>C NCBI36
NG_011488.2:g.25637A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*4960A>G MANE Select ENSP00000363157.3:n.*4960A>G
ENST00000374045.4:c.*4960A>G ENSP00000363157.3:n.*4960A>G
NM_001204344.1:c.5539A>G NP_001191273.1:n.5539A>G
NM_005118.3:c.*4960A>G NP_005109.2:n.*4960A>G
NM_005118.4:c.*4960A>G MANE Select NP_005109.2:n.*4960A>G
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