Canonical Allele Identifier: CA2672190288
Gene: IL15 HGNC NCBI

Linked Data

gnomAD v4: 4-141733299-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733299T>A , CM000666.2:g.141733299T>A GRCh38
NC_000004.11:g.142654452T>A , CM000666.1:g.142654452T>A GRCh37
NC_000004.10:g.142873902T>A NCBI36
NG_029605.1:g.101704T>A
NG_029605.2:g.101704T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*451T>A MANE Select ENSP00000323505.4:n.*451T>A
ENST00000296545.11:c.*451T>A ENSP00000296545.7:n.*451T>A
ENST00000320650.8:c.*451T>A ENSP00000323505.4:n.*451T>A
ENST00000394159.2:c.859T>A ENSP00000377714.1:n.859T>A
ENST00000477265.5:c.*451T>A ENSP00000436914.1:n.*451T>A
NM_000585.4:c.*451T>A NP_000576.1:n.*451T>A
NM_172175.2:c.*451T>A NP_751915.1:n.*451T>A
NR_037840.2:n.1790T>A
NM_000585.5:c.*451T>A MANE Select NP_000576.1:n.*451T>A
NM_172175.3:c.*451T>A NP_751915.1:n.*451T>A
NR_037840.3:n.1803T>A
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