Canonical Allele Identifier: CA116967256

Gene: IL7R

Linked Data

• ClinVar Variation Id: 1026887
• ClinVar RCV Id: RCV001327408
• dbSNP Id: rs201106853
• COSMIC: COSM1695577
• MyVariant Identifiers: chr5:g.35867493G>A (hg19) ; chr5:g.35867391G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867391G>A , CM000667.2:g.35867391G>A	GRCh38
NC_000005.9:g.35867493G>A , CM000667.1:g.35867493G>A	GRCh37
NC_000005.8:g.35903250G>A	NCBI36
NG_009567.1:g.15503G>A , LRG_74:g.15503G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.307G>A MANE Select	ENSP00000306157.3:p.Gly103Arg
ENST00000303115.7:c.307G>A	ENSP00000306157.3:p.Gly103Arg
ENST00000506850.5:c.307G>A	ENSP00000421207.1:p.Gly103Arg
ENST00000511031.1:n.441G>A
ENST00000511982.1:c.307G>A	ENSP00000425309.1:p.Gly103Arg
ENST00000514217.5:c.307G>A	ENSP00000427688.1:p.Gly103Arg
NM_002185.3:c.307G>A	NP_002176.2:p.Gly103Arg
NR_120485.1:n.410G>A
XM_005248299.2:c.307G>A	XP_005248356.1:p.Gly103Arg
XM_005248300.1:c.307G>A	XP_005248357.1:p.Gly103Arg
XM_011514037.1:c.307G>A	XP_011512339.1:p.Gly103Arg
NM_002185.4:c.307G>A	NP_002176.2:p.Gly103Arg
NR_120485.2:n.436G>A
XM_005248299.4:c.307G>A	XP_005248356.1:p.Gly103Arg
NM_002185.5:c.307G>A MANE Select	NP_002176.2:p.Gly103Arg
NR_120485.3:n.394G>A