Canonical Allele Identifier: CA555318055

Gene: IL15

Linked Data

• dbSNP Id: rs1458474294
• gnomAD v2: 4-142654402-G-A
• gnomAD v3: 4-141733249-G-A
• gnomAD v4: 4-141733249-G-A
• MyVariant Identifiers: chr4:g.142654402G>A (hg19) ; chr4:g.141733249G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733249G>A , CM000666.2:g.141733249G>A	GRCh38
NC_000004.11:g.142654402G>A , CM000666.1:g.142654402G>A	GRCh37
NC_000004.10:g.142873852G>A	NCBI36
NG_029605.1:g.101654G>A
NG_029605.2:g.101654G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*401G>A MANE Select	ENSP00000323505.4:n.*401G>A
ENST00000296545.11:c.*401G>A	ENSP00000296545.7:n.*401G>A
ENST00000320650.8:c.*401G>A	ENSP00000323505.4:n.*401G>A
ENST00000394159.2:c.809G>A	ENSP00000377714.1:n.809G>A
ENST00000477265.5:c.*401G>A	ENSP00000436914.1:n.*401G>A
NM_000585.4:c.*401G>A	NP_000576.1:n.*401G>A
NM_172175.2:c.*401G>A	NP_751915.1:n.*401G>A
NR_037840.2:n.1740G>A
NM_000585.5:c.*401G>A MANE Select	NP_000576.1:n.*401G>A
NM_172175.3:c.*401G>A	NP_751915.1:n.*401G>A
NR_037840.3:n.1753G>A