Canonical Allele Identifier: CA788196400

Gene: IL15

Linked Data

• dbSNP Id: rs1347386767
• gnomAD v3: 4-141732956-T-C
• gnomAD v4: 4-141732956-T-C
• MyVariant Identifiers: chr4:g.142654109T>C (hg19) ; chr4:g.141732956T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141732956T>C , CM000666.2:g.141732956T>C	GRCh38
NC_000004.11:g.142654109T>C , CM000666.1:g.142654109T>C	GRCh37
NC_000004.10:g.142873559T>C	NCBI36
NG_029605.1:g.101361T>C
NG_029605.2:g.101361T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*108T>C MANE Select	ENSP00000323505.4:n.*108T>C
ENST00000296545.11:c.*108T>C	ENSP00000296545.7:n.*108T>C
ENST00000320650.8:c.*108T>C	ENSP00000323505.4:n.*108T>C
ENST00000394159.2:c.516T>C	ENSP00000377714.1:n.516T>C
ENST00000477265.5:c.*108T>C	ENSP00000436914.1:n.*108T>C
ENST00000514653.5:c.*108T>C	ENSP00000422271.1:n.*108T>C
ENST00000529613.5:c.*108T>C	ENSP00000435462.1:n.*108T>C
NM_000585.4:c.*108T>C	NP_000576.1:n.*108T>C
NM_172175.2:c.*108T>C	NP_751915.1:n.*108T>C
NR_037840.2:n.1447T>C
NM_000585.5:c.*108T>C MANE Select	NP_000576.1:n.*108T>C
NM_172175.3:c.*108T>C	NP_751915.1:n.*108T>C
NR_037840.3:n.1460T>C