Canonical Allele Identifier: CA2707263861

Gene: IL15

Linked Data

• dbSNP Id: rs1730505876

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733079T>A , CM000666.2:g.141733079T>A	GRCh38
NC_000004.11:g.142654232T>A , CM000666.1:g.142654232T>A	GRCh37
NC_000004.10:g.142873682T>A	NCBI36
NG_029605.1:g.101484T>A
NG_029605.2:g.101484T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*231T>A MANE Select	ENSP00000323505.4:n.*231T>A
ENST00000296545.11:c.*231T>A	ENSP00000296545.7:n.*231T>A
ENST00000320650.8:c.*231T>A	ENSP00000323505.4:n.*231T>A
ENST00000394159.2:c.639T>A	ENSP00000377714.1:n.639T>A
ENST00000477265.5:c.*231T>A	ENSP00000436914.1:n.*231T>A
ENST00000514653.5:c.*231T>A	ENSP00000422271.1:n.*231T>A
ENST00000529613.5:c.*231T>A	ENSP00000435462.1:n.*231T>A
NM_000585.4:c.*231T>A	NP_000576.1:n.*231T>A
NM_172175.2:c.*231T>A	NP_751915.1:n.*231T>A
NR_037840.2:n.1570T>A
NM_000585.5:c.*231T>A MANE Select	NP_000576.1:n.*231T>A
NM_172175.3:c.*231T>A	NP_751915.1:n.*231T>A
NR_037840.3:n.1583T>A