Canonical Allele Identifier: CA1539080702
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35876172A= , CM000667.2:g.35876172A= GRCh38
NC_000005.9:g.35876274A= , CM000667.1:g.35876274A= GRCh37
NC_000005.8:g.35912031A= NCBI36
NG_009567.1:g.24284A= , LRG_74:g.24284A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.1066A= MANE Select ENSP00000306157.3:p.Ile356=
ENST00000303115.7:c.1066A= ENSP00000306157.3:p.Ile356=
ENST00000505093.1:c.381A= ENSP00000426069.1:n.381A=
ENST00000505875.1:n.364A=
ENST00000514217.5:c.*260A= ENSP00000427688.1:n.*260A=
NM_002185.3:c.1066A= NP_002176.2:p.Ile356=
NR_120485.1:n.906A=
NM_002185.4:c.1066A= NP_002176.2:p.Ile356=
NR_120485.2:n.932A=
XM_005248299.4:c.*183A= XP_005248356.1:n.*183A=
NM_002185.5:c.1066A= MANE Select NP_002176.2:p.Ile356=
NR_120485.3:n.890A=