Canonical Allele Identifier: CA116953176
Community Standard Title: NM_002185.5(IL7R):c.82+14A>T
Gene: IL7R HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35857073A>T , CM000667.2:g.35857073A>T GRCh38
NC_000005.9:g.35857175A>T , CM000667.1:g.35857175A>T GRCh37
NC_000005.8:g.35892932A>T NCBI36
NG_009567.1:g.5185A>T , LRG_74:g.5185A>T

Transcript Alleles

HGVS Amino-acid Change
NM_002185.5:c.82+14A>T MANE Select NP_002176.2:n.82+14A>T
ENST00000303115.8:c.82+14A>T MANE Select ENSP00000306157.3:n.82+14A>T
NM_002185.3:c.82+14A>T NP_002176.2:n.82+14A>T
NM_002185.4:c.82+14A>T NP_002176.2:n.82+14A>T
NR_120485.1:n.185+14A>T
NR_120485.2:n.211+14A>T
NR_120485.3:n.169+14A>T
ENST00000303115.7:c.82+14A>T ENSP00000306157.3:n.82+14A>T
ENST00000506850.5:c.82+14A>T ENSP00000421207.1:n.82+14A>T
ENST00000508941.5:c.82+14A>T ENSP00000426426.1:n.82+14A>T
ENST00000511031.1:n.217-3779A>T
ENST00000511982.1:c.82+14A>T ENSP00000425309.1:n.82+14A>T
ENST00000514217.5:c.82+14A>T ENSP00000427688.1:n.82+14A>T
ENST00000515665.1:c.82+14A>T ENSP00000425538.1:n.82+14A>T
XM_005248299.2:c.82+14A>T XP_005248356.1:n.82+14A>T
XM_005248299.4:c.82+14A>T XP_005248356.1:n.82+14A>T
XM_005248300.1:c.82+14A>T XP_005248357.1:n.82+14A>T
XM_011514037.1:c.82+14A>T XP_011512339.1:n.82+14A>T
XR_001742635.1:n.1533+1794T>A
Search 100 bp 5'
Search 100 bp 3'