Canonical Allele Identifier: CA788196433

Gene: IL15

Linked Data

• dbSNP Id: rs1264675935
• gnomAD v4: 4-141733014-A-G
• MyVariant Identifiers: chr4:g.142654167A>G (hg19) ; chr4:g.141733014A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733014A>G , CM000666.2:g.141733014A>G	GRCh38
NC_000004.11:g.142654167A>G , CM000666.1:g.142654167A>G	GRCh37
NC_000004.10:g.142873617A>G	NCBI36
NG_029605.1:g.101419A>G
NG_029605.2:g.101419A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*166A>G MANE Select	ENSP00000323505.4:n.*166A>G
ENST00000296545.11:c.*166A>G	ENSP00000296545.7:n.*166A>G
ENST00000320650.8:c.*166A>G	ENSP00000323505.4:n.*166A>G
ENST00000394159.2:c.574A>G	ENSP00000377714.1:n.574A>G
ENST00000477265.5:c.*166A>G	ENSP00000436914.1:n.*166A>G
ENST00000514653.5:c.*166A>G	ENSP00000422271.1:n.*166A>G
ENST00000529613.5:c.*166A>G	ENSP00000435462.1:n.*166A>G
NM_000585.4:c.*166A>G	NP_000576.1:n.*166A>G
NM_172175.2:c.*166A>G	NP_751915.1:n.*166A>G
NR_037840.2:n.1505A>G
NM_000585.5:c.*166A>G MANE Select	NP_000576.1:n.*166A>G
NM_172175.3:c.*166A>G	NP_751915.1:n.*166A>G
NR_037840.3:n.1518A>G