Canonical Allele Identifier: CA2672190298
Gene: IL15 HGNC NCBI

Linked Data

gnomAD v4: 4-141733304-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733304C>G , CM000666.2:g.141733304C>G GRCh38
NC_000004.11:g.142654457C>G , CM000666.1:g.142654457C>G GRCh37
NC_000004.10:g.142873907C>G NCBI36
NG_029605.1:g.101709C>G
NG_029605.2:g.101709C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320650.9:c.*456C>G MANE Select ENSP00000323505.4:n.*456C>G
ENST00000296545.11:c.*456C>G ENSP00000296545.7:n.*456C>G
ENST00000320650.8:c.*456C>G ENSP00000323505.4:n.*456C>G
ENST00000394159.2:c.864C>G ENSP00000377714.1:n.864C>G
ENST00000477265.5:c.*456C>G ENSP00000436914.1:n.*456C>G
NM_000585.4:c.*456C>G NP_000576.1:n.*456C>G
NM_172175.2:c.*456C>G NP_751915.1:n.*456C>G
NR_037840.2:n.1795C>G
NM_000585.5:c.*456C>G MANE Select NP_000576.1:n.*456C>G
NM_172175.3:c.*456C>G NP_751915.1:n.*456C>G
NR_037840.3:n.1808C>G
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