Canonical Allele Identifier: CA788196615

Gene: IL15

Linked Data

• dbSNP Id: rs10833
• MyVariant Identifiers: chr4:g.142654547T>A (hg19) ; chr4:g.141733394T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733394T>A , CM000666.2:g.141733394T>A	GRCh38
NC_000004.11:g.142654547T>A , CM000666.1:g.142654547T>A	GRCh37
NC_000004.10:g.142873997T>A	NCBI36
NG_029605.1:g.101799T>A
NG_029605.2:g.101799T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000320650.9:c.*546T>A MANE Select	ENSP00000323505.4:n.*546T>A
ENST00000296545.11:c.*546T>A	ENSP00000296545.7:n.*546T>A
ENST00000320650.8:c.*546T>A	ENSP00000323505.4:n.*546T>A
ENST00000394159.2:c.954T>A	ENSP00000377714.1:n.954T>A
ENST00000477265.5:c.*546T>A	ENSP00000436914.1:n.*546T>A
NM_000585.4:c.*546T>A	NP_000576.1:n.*546T>A
NM_172175.2:c.*546T>A	NP_751915.1:n.*546T>A
NR_037840.2:n.1885T>A
NM_000585.5:c.*546T>A MANE Select	NP_000576.1:n.*546T>A
NM_172175.3:c.*546T>A	NP_751915.1:n.*546T>A
NR_037840.3:n.1898T>A