Canonical Allele Identifier: CA359428626

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35867550G>T (hg19) ; chr5:g.35867448G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867448G>T , CM000667.2:g.35867448G>T	GRCh38
NC_000005.9:g.35867550G>T , CM000667.1:g.35867550G>T	GRCh37
NC_000005.8:g.35903307G>T	NCBI36
NG_009567.1:g.15560G>T , LRG_74:g.15560G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.364G>T MANE Select	ENSP00000306157.3:p.Asp122Tyr
ENST00000303115.7:c.364G>T	ENSP00000306157.3:p.Asp122Tyr
ENST00000506850.5:c.364G>T	ENSP00000421207.1:p.Asp122Tyr
ENST00000511031.1:n.498G>T
ENST00000511982.1:c.364G>T	ENSP00000425309.1:p.Asp122Tyr
ENST00000514217.5:c.364G>T	ENSP00000427688.1:p.Asp122Tyr
NM_002185.3:c.364G>T	NP_002176.2:p.Asp122Tyr
NR_120485.1:n.467G>T
XM_005248299.2:c.364G>T	XP_005248356.1:p.Asp122Tyr
XM_005248300.1:c.364G>T	XP_005248357.1:p.Asp122Tyr
XM_011514037.1:c.364G>T	XP_011512339.1:p.Asp122Tyr
NM_002185.4:c.364G>T	NP_002176.2:p.Asp122Tyr
NR_120485.2:n.493G>T
XM_005248299.4:c.364G>T	XP_005248356.1:p.Asp122Tyr
NM_002185.5:c.364G>T MANE Select	NP_002176.2:p.Asp122Tyr
NR_120485.3:n.451G>T