Canonical Allele Identifier: CA107424332
Gene: IL15 HGNC NCBI

Linked Data

dbSNP Id: rs577213864
MyVariant Identifiers: chr4:g.142654559G>C (hg19) chr4:g.141733406G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733406G>C , CM000666.2:g.141733406G>C GRCh38
NC_000004.11:g.142654559G>C , CM000666.1:g.142654559G>C GRCh37
NC_000004.10:g.142874009G>C NCBI36
NG_029605.1:g.101811G>C
NG_029605.2:g.101811G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320650.9:c.*558G>C MANE Select ENSP00000323505.4:n.*558G>C
ENST00000296545.11:c.*558G>C ENSP00000296545.7:n.*558G>C
ENST00000320650.8:c.*558G>C ENSP00000323505.4:n.*558G>C
ENST00000394159.2:c.966G>C ENSP00000377714.1:n.966G>C
ENST00000477265.5:c.*558G>C ENSP00000436914.1:n.*558G>C
NM_000585.4:c.*558G>C NP_000576.1:n.*558G>C
NM_172175.2:c.*558G>C NP_751915.1:n.*558G>C
NR_037840.2:n.1897G>C
NM_000585.5:c.*558G>C MANE Select NP_000576.1:n.*558G>C
NM_172175.3:c.*558G>C NP_751915.1:n.*558G>C
NR_037840.3:n.1910G>C
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