Canonical Allele Identifier: CA2672190355
Gene: IL15 HGNC NCBI

Linked Data

gnomAD v4: 4-141733400-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733400A>C , CM000666.2:g.141733400A>C GRCh38
NC_000004.11:g.142654553A>C , CM000666.1:g.142654553A>C GRCh37
NC_000004.10:g.142874003A>C NCBI36
NG_029605.1:g.101805A>C
NG_029605.2:g.101805A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320650.9:c.*552A>C MANE Select ENSP00000323505.4:n.*552A>C
ENST00000296545.11:c.*552A>C ENSP00000296545.7:n.*552A>C
ENST00000320650.8:c.*552A>C ENSP00000323505.4:n.*552A>C
ENST00000394159.2:c.960A>C ENSP00000377714.1:n.960A>C
ENST00000477265.5:c.*552A>C ENSP00000436914.1:n.*552A>C
NM_000585.4:c.*552A>C NP_000576.1:n.*552A>C
NM_172175.2:c.*552A>C NP_751915.1:n.*552A>C
NR_037840.2:n.1891A>C
NM_000585.5:c.*552A>C MANE Select NP_000576.1:n.*552A>C
NM_172175.3:c.*552A>C NP_751915.1:n.*552A>C
NR_037840.3:n.1904A>C
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