Canonical Allele Identifier: CA1068842247

Gene: IL15

Linked Data

• dbSNP Id: rs1730501761
• gnomAD v3: 4-141732965-A-G
• gnomAD v4: 4-141732965-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732965A>G , CM000666.2:g.141732965A>G	GRCh38
NC_000004.11:g.142654118A>G , CM000666.1:g.142654118A>G	GRCh37
NC_000004.10:g.142873568A>G	NCBI36
NG_029605.1:g.101370A>G
NG_029605.2:g.101370A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*117A>G MANE Select	ENSP00000323505.4:n.*117A>G
ENST00000296545.11:c.*117A>G	ENSP00000296545.7:n.*117A>G
ENST00000320650.8:c.*117A>G	ENSP00000323505.4:n.*117A>G
ENST00000394159.2:c.525A>G	ENSP00000377714.1:n.525A>G
ENST00000477265.5:c.*117A>G	ENSP00000436914.1:n.*117A>G
ENST00000514653.5:c.*117A>G	ENSP00000422271.1:n.*117A>G
ENST00000529613.5:c.*117A>G	ENSP00000435462.1:n.*117A>G
NM_000585.4:c.*117A>G	NP_000576.1:n.*117A>G
NM_172175.2:c.*117A>G	NP_751915.1:n.*117A>G
NR_037840.2:n.1456A>G
NM_000585.5:c.*117A>G MANE Select	NP_000576.1:n.*117A>G
NM_172175.3:c.*117A>G	NP_751915.1:n.*117A>G
NR_037840.3:n.1469A>G