Canonical Allele Identifier: CA788196556

Gene: IL15

Linked Data

• dbSNP Id: rs1421967093
• gnomAD v3: 4-141733298-C-A
• gnomAD v4: 4-141733298-C-A
• MyVariant Identifiers: chr4:g.142654451C>A (hg19) ; chr4:g.141733298C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733298C>A , CM000666.2:g.141733298C>A	GRCh38
NC_000004.11:g.142654451C>A , CM000666.1:g.142654451C>A	GRCh37
NC_000004.10:g.142873901C>A	NCBI36
NG_029605.1:g.101703C>A
NG_029605.2:g.101703C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*450C>A MANE Select	ENSP00000323505.4:n.*450C>A
ENST00000296545.11:c.*450C>A	ENSP00000296545.7:n.*450C>A
ENST00000320650.8:c.*450C>A	ENSP00000323505.4:n.*450C>A
ENST00000394159.2:c.858C>A	ENSP00000377714.1:n.858C>A
ENST00000477265.5:c.*450C>A	ENSP00000436914.1:n.*450C>A
NM_000585.4:c.*450C>A	NP_000576.1:n.*450C>A
NM_172175.2:c.*450C>A	NP_751915.1:n.*450C>A
NR_037840.2:n.1789C>A
NM_000585.5:c.*450C>A MANE Select	NP_000576.1:n.*450C>A
NM_172175.3:c.*450C>A	NP_751915.1:n.*450C>A
NR_037840.3:n.1802C>A