Canonical Allele Identifier: CA2672190353
Gene: IL15 HGNC NCBI

Linked Data

gnomAD v4: 4-141733398-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733398G>C , CM000666.2:g.141733398G>C GRCh38
NC_000004.11:g.142654551G>C , CM000666.1:g.142654551G>C GRCh37
NC_000004.10:g.142874001G>C NCBI36
NG_029605.1:g.101803G>C
NG_029605.2:g.101803G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320650.9:c.*550G>C MANE Select ENSP00000323505.4:n.*550G>C
ENST00000296545.11:c.*550G>C ENSP00000296545.7:n.*550G>C
ENST00000320650.8:c.*550G>C ENSP00000323505.4:n.*550G>C
ENST00000394159.2:c.958G>C ENSP00000377714.1:n.958G>C
ENST00000477265.5:c.*550G>C ENSP00000436914.1:n.*550G>C
NM_000585.4:c.*550G>C NP_000576.1:n.*550G>C
NM_172175.2:c.*550G>C NP_751915.1:n.*550G>C
NR_037840.2:n.1889G>C
NM_000585.5:c.*550G>C MANE Select NP_000576.1:n.*550G>C
NM_172175.3:c.*550G>C NP_751915.1:n.*550G>C
NR_037840.3:n.1902G>C
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