Canonical Allele Identifier: CA788196411

Gene: IL15

Linked Data

• dbSNP Id: rs1404456467
• gnomAD v4: 4-141732966-A-T
• MyVariant Identifiers: chr4:g.142654119A>T (hg19) ; chr4:g.141732966A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732966A>T , CM000666.2:g.141732966A>T	GRCh38
NC_000004.11:g.142654119A>T , CM000666.1:g.142654119A>T	GRCh37
NC_000004.10:g.142873569A>T	NCBI36
NG_029605.1:g.101371A>T
NG_029605.2:g.101371A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*118A>T MANE Select	ENSP00000323505.4:n.*118A>T
ENST00000296545.11:c.*118A>T	ENSP00000296545.7:n.*118A>T
ENST00000320650.8:c.*118A>T	ENSP00000323505.4:n.*118A>T
ENST00000394159.2:c.526A>T	ENSP00000377714.1:n.526A>T
ENST00000477265.5:c.*118A>T	ENSP00000436914.1:n.*118A>T
ENST00000514653.5:c.*118A>T	ENSP00000422271.1:n.*118A>T
ENST00000529613.5:c.*118A>T	ENSP00000435462.1:n.*118A>T
NM_000585.4:c.*118A>T	NP_000576.1:n.*118A>T
NM_172175.2:c.*118A>T	NP_751915.1:n.*118A>T
NR_037840.2:n.1457A>T
NM_000585.5:c.*118A>T MANE Select	NP_000576.1:n.*118A>T
NM_172175.3:c.*118A>T	NP_751915.1:n.*118A>T
NR_037840.3:n.1470A>T