Canonical Allele Identifier: CA104790279
Gene: IL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122452742G>A , CM000666.2:g.122452742G>A GRCh38
NC_000004.11:g.123373897G>A , CM000666.1:g.123373897G>A GRCh37
NC_000004.10:g.123593347G>A NCBI36
NG_016779.1:g.8754C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226730.5:c.352-880C>T MANE Select ENSP00000226730.5:n.352-880C>T
ENST00000226730.4:c.352-880C>T ENSP00000226730.4:n.352-880C>T
ENST00000477645.1:n.442-880C>T
NM_000586.3:c.352-880C>T NP_000577.2:n.352-880C>T
XM_017008177.1:c.351+968C>T XP_016863666.1:n.351+968C>T
NM_000586.4:c.352-880C>T MANE Select NP_000577.2:n.352-880C>T