Canonical Allele Identifier: CA3231904
Gene: IL7R HGNC NCBI

Linked Data

dbSNP Id: rs771757728
gnomAD v2: 5-35867486-A-T
gnomAD v4: 5-35867384-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867384A>T , CM000667.2:g.35867384A>T GRCh38
NC_000005.9:g.35867486A>T , CM000667.1:g.35867486A>T GRCh37
NC_000005.8:g.35903243A>T NCBI36
NG_009567.1:g.15496A>T , LRG_74:g.15496A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.300A>T MANE Select ENSP00000306157.3:p.Leu100Phe
ENST00000303115.7:c.300A>T ENSP00000306157.3:p.Leu100Phe
ENST00000506850.5:c.300A>T ENSP00000421207.1:p.Leu100Phe
ENST00000511031.1:n.434A>T
ENST00000511982.1:c.300A>T ENSP00000425309.1:p.Leu100Phe
ENST00000514217.5:c.300A>T ENSP00000427688.1:p.Leu100Phe
NM_002185.3:c.300A>T NP_002176.2:p.Leu100Phe
NR_120485.1:n.403A>T
XM_005248299.2:c.300A>T XP_005248356.1:p.Leu100Phe
XM_005248300.1:c.300A>T XP_005248357.1:p.Leu100Phe
XM_011514037.1:c.300A>T XP_011512339.1:p.Leu100Phe
NM_002185.4:c.300A>T NP_002176.2:p.Leu100Phe
NR_120485.2:n.429A>T
XM_005248299.4:c.300A>T XP_005248356.1:p.Leu100Phe
NM_002185.5:c.300A>T MANE Select NP_002176.2:p.Leu100Phe
NR_120485.3:n.387A>T