Canonical Allele Identifier: CA107424334

Gene: IL15

Linked Data

• dbSNP Id: rs535341302
• gnomAD v3: 4-141733418-T-C
• gnomAD v4: 4-141733418-T-C
• MyVariant Identifiers: chr4:g.142654571T>C (hg19) ; chr4:g.141733418T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141733418T>C , CM000666.2:g.141733418T>C	GRCh38
NC_000004.11:g.142654571T>C , CM000666.1:g.142654571T>C	GRCh37
NC_000004.10:g.142874021T>C	NCBI36
NG_029605.1:g.101823T>C
NG_029605.2:g.101823T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320650.9:c.*570T>C MANE Select	ENSP00000323505.4:n.*570T>C
ENST00000296545.11:c.*570T>C	ENSP00000296545.7:n.*570T>C
ENST00000320650.8:c.*570T>C	ENSP00000323505.4:n.*570T>C
ENST00000394159.2:c.978T>C	ENSP00000377714.1:n.978T>C
ENST00000477265.5:c.*570T>C	ENSP00000436914.1:n.*570T>C
NM_000585.4:c.*570T>C	NP_000576.1:n.*570T>C
NM_172175.2:c.*570T>C	NP_751915.1:n.*570T>C
NR_037840.2:n.1909T>C
NM_000585.5:c.*570T>C MANE Select	NP_000576.1:n.*570T>C
NM_172175.3:c.*570T>C	NP_751915.1:n.*570T>C
NR_037840.3:n.1922T>C