Canonical Allele Identifier: CA555318059

Gene: IL15

Linked Data

• dbSNP Id: rs1163920732
• gnomAD v2: 4-142654444-C-G
• gnomAD v3: 4-141733291-C-G
• gnomAD v4: 4-141733291-C-G
• MyVariant Identifiers: chr4:g.142654444C>G (hg19) ; chr4:g.141733291C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733291C>G , CM000666.2:g.141733291C>G	GRCh38
NC_000004.11:g.142654444C>G , CM000666.1:g.142654444C>G	GRCh37
NC_000004.10:g.142873894C>G	NCBI36
NG_029605.1:g.101696C>G
NG_029605.2:g.101696C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*443C>G MANE Select	ENSP00000323505.4:n.*443C>G
ENST00000296545.11:c.*443C>G	ENSP00000296545.7:n.*443C>G
ENST00000320650.8:c.*443C>G	ENSP00000323505.4:n.*443C>G
ENST00000394159.2:c.851C>G	ENSP00000377714.1:n.851C>G
ENST00000477265.5:c.*443C>G	ENSP00000436914.1:n.*443C>G
NM_000585.4:c.*443C>G	NP_000576.1:n.*443C>G
NM_172175.2:c.*443C>G	NP_751915.1:n.*443C>G
NR_037840.2:n.1782C>G
NM_000585.5:c.*443C>G MANE Select	NP_000576.1:n.*443C>G
NM_172175.3:c.*443C>G	NP_751915.1:n.*443C>G
NR_037840.3:n.1795C>G