Canonical Allele Identifier: CA3231888

Gene: IL7R

Linked Data

• ClinVar Variation Id: 1962818
• ClinVar RCV Id: RCV002710698
• dbSNP Id: rs139835773
• ExAC: 5:35867388 T / A
• gnomAD v2: 5-35867388-T-A
• gnomAD v3: 5-35867286-T-A
• gnomAD v4: 5-35867286-T-A
• MyVariant Identifiers: chr5:g.35867388T>A (hg19) ; chr5:g.35867286T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867286T>A , CM000667.2:g.35867286T>A	GRCh38
NC_000005.9:g.35867388T>A , CM000667.1:g.35867388T>A	GRCh37
NC_000005.8:g.35903145T>A	NCBI36
NG_009567.1:g.15398T>A , LRG_74:g.15398T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.222-20T>A MANE Select	ENSP00000306157.3:n.222-20T>A
ENST00000303115.7:c.222-20T>A	ENSP00000306157.3:n.222-20T>A
ENST00000506850.5:c.222-20T>A	ENSP00000421207.1:n.222-20T>A
ENST00000511031.1:n.356-20T>A
ENST00000511982.1:c.222-20T>A	ENSP00000425309.1:n.222-20T>A
ENST00000514217.5:c.222-20T>A	ENSP00000427688.1:n.222-20T>A
NM_002185.3:c.222-20T>A	NP_002176.2:n.222-20T>A
NR_120485.1:n.325-20T>A
XM_005248299.2:c.222-20T>A	XP_005248356.1:n.222-20T>A
XM_005248300.1:c.222-20T>A	XP_005248357.1:n.222-20T>A
XM_011514037.1:c.222-20T>A	XP_011512339.1:n.222-20T>A
NM_002185.4:c.222-20T>A	NP_002176.2:n.222-20T>A
NR_120485.2:n.351-20T>A
XM_005248299.4:c.222-20T>A	XP_005248356.1:n.222-20T>A
NM_002185.5:c.222-20T>A MANE Select	NP_002176.2:n.222-20T>A
NR_120485.3:n.309-20T>A