Canonical Allele Identifier: CA2672190372

Gene: IL15

Linked Data

• gnomAD v4: 4-141733417-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733417A>G , CM000666.2:g.141733417A>G	GRCh38
NC_000004.11:g.142654570A>G , CM000666.1:g.142654570A>G	GRCh37
NC_000004.10:g.142874020A>G	NCBI36
NG_029605.1:g.101822A>G
NG_029605.2:g.101822A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*569A>G MANE Select	ENSP00000323505.4:n.*569A>G
ENST00000296545.11:c.*569A>G	ENSP00000296545.7:n.*569A>G
ENST00000320650.8:c.*569A>G	ENSP00000323505.4:n.*569A>G
ENST00000394159.2:c.977A>G	ENSP00000377714.1:n.977A>G
ENST00000477265.5:c.*569A>G	ENSP00000436914.1:n.*569A>G
NM_000585.4:c.*569A>G	NP_000576.1:n.*569A>G
NM_172175.2:c.*569A>G	NP_751915.1:n.*569A>G
NR_037840.2:n.1908A>G
NM_000585.5:c.*569A>G MANE Select	NP_000576.1:n.*569A>G
NM_172175.3:c.*569A>G	NP_751915.1:n.*569A>G
NR_037840.3:n.1921A>G