Canonical Allele Identifier: CA15310377
Gene: IL15 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.141717598T>G
GRCh37 chr4:g.142638751T>G
gnomAD v2:
4:142638751 T / G
gnomAD v3:
4:141717598 T / G
gnomAD v4:
chr4-141717598-T-G
Joint Max Group AF 0.57499425 (SAS)
Genomes Max Group AF 0.575028 (SAS)
Exomes Max Group AF 0.43591559 (NFE)
dbSNP:
6819823
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141717598T>G , CM000666.2:g.141717598T>G GRCh38
NC_000004.11:g.142638751T>G , CM000666.1:g.142638751T>G GRCh37
NC_000004.10:g.142858201T>G NCBI36
NG_029605.1:g.86003T>G
NG_029605.2:g.86003T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.-99-1768T>G MANE Select ENSP00000323505.4:n.-99-1768T>G
ENST00000296545.11:c.-99-1768T>G ENSP00000296545.7:n.-99-1768T>G
ENST00000320650.8:c.-99-1768T>G ENSP00000323505.4:n.-99-1768T>G
ENST00000477265.5:c.-2067T>G ENSP00000436914.1:n.-2067T>G
ENST00000514653.5:c.-287-1780T>G ENSP00000422271.1:n.-287-1780T>G
ENST00000529613.5:c.-99-1768T>G ENSP00000435462.1:n.-99-1768T>G
NM_000585.4:c.-99-1768T>G NP_000576.1:n.-99-1768T>G
NM_172175.2:c.-287-1780T>G NP_751915.1:n.-287-1780T>G
NR_037840.2:n.752-1768T>G
NM_000585.5:c.-99-1768T>G MANE Select NP_000576.1:n.-99-1768T>G
NM_172175.3:c.-287-1780T>G NP_751915.1:n.-287-1780T>G
NR_037840.3:n.765-1768T>G
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