Canonical Allele Identifier: CA2673534976
Gene: IL7R HGNC NCBI

Linked Data

gnomAD v4: 5-35867586-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35867586A>C , CM000667.2:g.35867586A>C GRCh38
NC_000005.9:g.35867688A>C , CM000667.1:g.35867688A>C GRCh37
NC_000005.8:g.35903445A>C NCBI36
NG_009567.1:g.15698A>C , LRG_74:g.15698A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.379+123A>C MANE Select ENSP00000306157.3:n.379+123A>C
ENST00000303115.7:c.379+123A>C ENSP00000306157.3:n.379+123A>C
ENST00000506850.5:c.379+123A>C ENSP00000421207.1:n.379+123A>C
ENST00000511982.1:c.*49A>C ENSP00000425309.1:n.*49A>C
ENST00000514217.5:c.379+123A>C ENSP00000427688.1:n.379+123A>C
NM_002185.3:c.379+123A>C NP_002176.2:n.379+123A>C
NR_120485.1:n.482+123A>C
XM_005248299.2:c.379+123A>C XP_005248356.1:n.379+123A>C
XM_005248300.1:c.379+123A>C XP_005248357.1:n.379+123A>C
XM_011514037.1:c.379+123A>C XP_011512339.1:n.379+123A>C
NM_002185.4:c.379+123A>C NP_002176.2:n.379+123A>C
NR_120485.2:n.508+123A>C
XM_005248299.4:c.379+123A>C XP_005248356.1:n.379+123A>C
NM_002185.5:c.379+123A>C MANE Select NP_002176.2:n.379+123A>C
NR_120485.3:n.466+123A>C