Canonical Allele Identifier: CA359428482

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35867520G>A (hg19) ; chr5:g.35867418G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867418G>A , CM000667.2:g.35867418G>A	GRCh38
NC_000005.9:g.35867520G>A , CM000667.1:g.35867520G>A	GRCh37
NC_000005.8:g.35903277G>A	NCBI36
NG_009567.1:g.15530G>A , LRG_74:g.15530G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.334G>A MANE Select	ENSP00000306157.3:p.Gly112Arg
ENST00000303115.7:c.334G>A	ENSP00000306157.3:p.Gly112Arg
ENST00000506850.5:c.334G>A	ENSP00000421207.1:p.Gly112Arg
ENST00000511031.1:n.468G>A
ENST00000511982.1:c.334G>A	ENSP00000425309.1:p.Gly112Arg
ENST00000514217.5:c.334G>A	ENSP00000427688.1:p.Gly112Arg
NM_002185.3:c.334G>A	NP_002176.2:p.Gly112Arg
NR_120485.1:n.437G>A
XM_005248299.2:c.334G>A	XP_005248356.1:p.Gly112Arg
XM_005248300.1:c.334G>A	XP_005248357.1:p.Gly112Arg
XM_011514037.1:c.334G>A	XP_011512339.1:p.Gly112Arg
NM_002185.4:c.334G>A	NP_002176.2:p.Gly112Arg
NR_120485.2:n.463G>A
XM_005248299.4:c.334G>A	XP_005248356.1:p.Gly112Arg
NM_002185.5:c.334G>A MANE Select	NP_002176.2:p.Gly112Arg
NR_120485.3:n.421G>A