Canonical Allele Identifier: CA11894717
Gene: IL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122454980G>A , CM000666.2:g.122454980G>A GRCh38
NC_000004.11:g.123376135G>A , CM000666.1:g.123376135G>A GRCh37
NC_000004.10:g.123595585G>A NCBI36
NG_016779.1:g.6516C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226730.5:c.208-1127C>T MANE Select ENSP00000226730.5:n.208-1127C>T
ENST00000226730.4:c.208-1127C>T ENSP00000226730.4:n.208-1127C>T
ENST00000477645.1:n.298-1127C>T
NM_000586.3:c.208-1127C>T NP_000577.2:n.208-1127C>T
XM_017008177.1:c.208-1127C>T XP_016863666.1:n.208-1127C>T
NM_000586.4:c.208-1127C>T MANE Select NP_000577.2:n.208-1127C>T