Canonical Allele Identifier: CA788196624
Gene: IL15 HGNC NCBI

Linked Data

dbSNP Id: rs1490568446
gnomAD v4: 4-141733408-T-C
MyVariant Identifiers: chr4:g.142654561T>C (hg19) chr4:g.141733408T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733408T>C , CM000666.2:g.141733408T>C GRCh38
NC_000004.11:g.142654561T>C , CM000666.1:g.142654561T>C GRCh37
NC_000004.10:g.142874011T>C NCBI36
NG_029605.1:g.101813T>C
NG_029605.2:g.101813T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320650.9:c.*560T>C MANE Select ENSP00000323505.4:n.*560T>C
ENST00000296545.11:c.*560T>C ENSP00000296545.7:n.*560T>C
ENST00000320650.8:c.*560T>C ENSP00000323505.4:n.*560T>C
ENST00000394159.2:c.968T>C ENSP00000377714.1:n.968T>C
ENST00000477265.5:c.*560T>C ENSP00000436914.1:n.*560T>C
NM_000585.4:c.*560T>C NP_000576.1:n.*560T>C
NM_172175.2:c.*560T>C NP_751915.1:n.*560T>C
NR_037840.2:n.1899T>C
NM_000585.5:c.*560T>C MANE Select NP_000576.1:n.*560T>C
NM_172175.3:c.*560T>C NP_751915.1:n.*560T>C
NR_037840.3:n.1912T>C
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