Canonical Allele Identifier: CA2672190308
Gene: IL15 HGNC NCBI

Linked Data

gnomAD v4: 4-141733321-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733321T>C , CM000666.2:g.141733321T>C GRCh38
NC_000004.11:g.142654474T>C , CM000666.1:g.142654474T>C GRCh37
NC_000004.10:g.142873924T>C NCBI36
NG_029605.1:g.101726T>C
NG_029605.2:g.101726T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*473T>C MANE Select ENSP00000323505.4:n.*473T>C
ENST00000296545.11:c.*473T>C ENSP00000296545.7:n.*473T>C
ENST00000320650.8:c.*473T>C ENSP00000323505.4:n.*473T>C
ENST00000394159.2:c.881T>C ENSP00000377714.1:n.881T>C
ENST00000477265.5:c.*473T>C ENSP00000436914.1:n.*473T>C
NM_000585.4:c.*473T>C NP_000576.1:n.*473T>C
NM_172175.2:c.*473T>C NP_751915.1:n.*473T>C
NR_037840.2:n.1812T>C
NM_000585.5:c.*473T>C MANE Select NP_000576.1:n.*473T>C
NM_172175.3:c.*473T>C NP_751915.1:n.*473T>C
NR_037840.3:n.1825T>C
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