Canonical Allele Identifier: CA107424333

Gene: IL15

Linked Data

• dbSNP Id: rs996298997
• gnomAD v4: 4-141733413-A-G
• MyVariant Identifiers: chr4:g.142654566A>G (hg19) ; chr4:g.141733413A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733413A>G , CM000666.2:g.141733413A>G	GRCh38
NC_000004.11:g.142654566A>G , CM000666.1:g.142654566A>G	GRCh37
NC_000004.10:g.142874016A>G	NCBI36
NG_029605.1:g.101818A>G
NG_029605.2:g.101818A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000320650.9:c.*565A>G MANE Select	ENSP00000323505.4:n.*565A>G
ENST00000296545.11:c.*565A>G	ENSP00000296545.7:n.*565A>G
ENST00000320650.8:c.*565A>G	ENSP00000323505.4:n.*565A>G
ENST00000394159.2:c.973A>G	ENSP00000377714.1:n.973A>G
ENST00000477265.5:c.*565A>G	ENSP00000436914.1:n.*565A>G
NM_000585.4:c.*565A>G	NP_000576.1:n.*565A>G
NM_172175.2:c.*565A>G	NP_751915.1:n.*565A>G
NR_037840.2:n.1904A>G
NM_000585.5:c.*565A>G MANE Select	NP_000576.1:n.*565A>G
NM_172175.3:c.*565A>G	NP_751915.1:n.*565A>G
NR_037840.3:n.1917A>G