Canonical Allele Identifier: CA788196577
Gene: IL15 HGNC NCBI

Linked Data

dbSNP Id: rs1360521571
gnomAD v4: 4-141733319-A-G
MyVariant Identifiers: chr4:g.142654472A>G (hg19) chr4:g.141733319A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141733319A>G , CM000666.2:g.141733319A>G GRCh38
NC_000004.11:g.142654472A>G , CM000666.1:g.142654472A>G GRCh37
NC_000004.10:g.142873922A>G NCBI36
NG_029605.1:g.101724A>G
NG_029605.2:g.101724A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320650.9:c.*471A>G MANE Select ENSP00000323505.4:n.*471A>G
ENST00000296545.11:c.*471A>G ENSP00000296545.7:n.*471A>G
ENST00000320650.8:c.*471A>G ENSP00000323505.4:n.*471A>G
ENST00000394159.2:c.879A>G ENSP00000377714.1:n.879A>G
ENST00000477265.5:c.*471A>G ENSP00000436914.1:n.*471A>G
NM_000585.4:c.*471A>G NP_000576.1:n.*471A>G
NM_172175.2:c.*471A>G NP_751915.1:n.*471A>G
NR_037840.2:n.1810A>G
NM_000585.5:c.*471A>G MANE Select NP_000576.1:n.*471A>G
NM_172175.3:c.*471A>G NP_751915.1:n.*471A>G
NR_037840.3:n.1823A>G
Search 100 bp 5'
Search 100 bp 3'