Canonical Allele Identifier: CA2672190346
Gene: IL15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733395A>T , CM000666.2:g.141733395A>T GRCh38
NC_000004.11:g.142654548A>T , CM000666.1:g.142654548A>T GRCh37
NC_000004.10:g.142873998A>T NCBI36
NG_029605.1:g.101800A>T
NG_029605.2:g.101800A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320650.9:c.*547A>T MANE Select ENSP00000323505.4:n.*547A>T
ENST00000296545.11:c.*547A>T ENSP00000296545.7:n.*547A>T
ENST00000320650.8:c.*547A>T ENSP00000323505.4:n.*547A>T
ENST00000394159.2:c.955A>T ENSP00000377714.1:n.955A>T
ENST00000477265.5:c.*547A>T ENSP00000436914.1:n.*547A>T
NM_000585.4:c.*547A>T NP_000576.1:n.*547A>T
NM_172175.2:c.*547A>T NP_751915.1:n.*547A>T
NR_037840.2:n.1886A>T
NM_000585.5:c.*547A>T MANE Select NP_000576.1:n.*547A>T
NM_172175.3:c.*547A>T NP_751915.1:n.*547A>T
NR_037840.3:n.1899A>T