Canonical Allele Identifier: CA2672190368
Gene: IL15 HGNC NCBI

Linked Data

gnomAD v4: 4-141733410-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733410T>A , CM000666.2:g.141733410T>A GRCh38
NC_000004.11:g.142654563T>A , CM000666.1:g.142654563T>A GRCh37
NC_000004.10:g.142874013T>A NCBI36
NG_029605.1:g.101815T>A
NG_029605.2:g.101815T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*562T>A MANE Select ENSP00000323505.4:n.*562T>A
ENST00000296545.11:c.*562T>A ENSP00000296545.7:n.*562T>A
ENST00000320650.8:c.*562T>A ENSP00000323505.4:n.*562T>A
ENST00000394159.2:c.970T>A ENSP00000377714.1:n.970T>A
ENST00000477265.5:c.*562T>A ENSP00000436914.1:n.*562T>A
NM_000585.4:c.*562T>A NP_000576.1:n.*562T>A
NM_172175.2:c.*562T>A NP_751915.1:n.*562T>A
NR_037840.2:n.1901T>A
NM_000585.5:c.*562T>A MANE Select NP_000576.1:n.*562T>A
NM_172175.3:c.*562T>A NP_751915.1:n.*562T>A
NR_037840.3:n.1914T>A
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