Canonical Allele Identifier: CA444093230
Gene: IL7R HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.35867456G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867354G>A , CM000667.2:g.35867354G>A GRCh38
NC_000005.9:g.35867456G>A , CM000667.1:g.35867456G>A GRCh37
NC_000005.8:g.35903213G>A NCBI36
NG_009567.1:g.15466G>A , LRG_74:g.15466G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.270G>A MANE Select ENSP00000306157.3:p.Glu90=
ENST00000303115.7:c.270G>A ENSP00000306157.3:p.Glu90=
ENST00000506850.5:c.270G>A ENSP00000421207.1:p.Glu90=
ENST00000511031.1:n.404G>A
ENST00000511982.1:c.270G>A ENSP00000425309.1:p.Glu90=
ENST00000514217.5:c.270G>A ENSP00000427688.1:p.Glu90=
NM_002185.3:c.270G>A NP_002176.2:p.Glu90=
NR_120485.1:n.373G>A
XM_005248299.2:c.270G>A XP_005248356.1:p.Glu90=
XM_005248300.1:c.270G>A XP_005248357.1:p.Glu90=
XM_011514037.1:c.270G>A XP_011512339.1:p.Glu90=
NM_002185.4:c.270G>A NP_002176.2:p.Glu90=
NR_120485.2:n.399G>A
XM_005248299.4:c.270G>A XP_005248356.1:p.Glu90=
NM_002185.5:c.270G>A MANE Select NP_002176.2:p.Glu90=
NR_120485.3:n.357G>A