Canonical Allele Identifier: CA107424330

Gene: IL15

Linked Data

• dbSNP Id: rs1018974722
• gnomAD v2: 4-142654550-T-G
• gnomAD v3: 4-141733397-T-G
• gnomAD v4: 4-141733397-T-G
• MyVariant Identifiers: chr4:g.142654550T>G (hg19) ; chr4:g.141733397T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733397T>G , CM000666.2:g.141733397T>G	GRCh38
NC_000004.11:g.142654550T>G , CM000666.1:g.142654550T>G	GRCh37
NC_000004.10:g.142874000T>G	NCBI36
NG_029605.1:g.101802T>G
NG_029605.2:g.101802T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*549T>G MANE Select	ENSP00000323505.4:n.*549T>G
ENST00000296545.11:c.*549T>G	ENSP00000296545.7:n.*549T>G
ENST00000320650.8:c.*549T>G	ENSP00000323505.4:n.*549T>G
ENST00000394159.2:c.957T>G	ENSP00000377714.1:n.957T>G
ENST00000477265.5:c.*549T>G	ENSP00000436914.1:n.*549T>G
NM_000585.4:c.*549T>G	NP_000576.1:n.*549T>G
NM_172175.2:c.*549T>G	NP_751915.1:n.*549T>G
NR_037840.2:n.1888T>G
NM_000585.5:c.*549T>G MANE Select	NP_000576.1:n.*549T>G
NM_172175.3:c.*549T>G	NP_751915.1:n.*549T>G
NR_037840.3:n.1901T>G