Canonical Allele Identifier: CA1539065823

Gene: IL7R

Linked Data

• dbSNP Id: rs1759695116

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35857760C>T , CM000667.2:g.35857760C>T	GRCh38
NC_000005.9:g.35857862C>T , CM000667.1:g.35857862C>T	GRCh37
NC_000005.8:g.35893619C>T	NCBI36
NG_009567.1:g.5872C>T , LRG_74:g.5872C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.82+701C>T MANE Select	ENSP00000306157.3:n.82+701C>T
ENST00000303115.7:c.82+701C>T	ENSP00000306157.3:n.82+701C>T
ENST00000506850.5:c.82+701C>T	ENSP00000421207.1:n.82+701C>T
ENST00000508941.5:c.82+701C>T	ENSP00000426426.1:n.82+701C>T
ENST00000511031.1:n.217-3092C>T
ENST00000511982.1:c.82+701C>T	ENSP00000425309.1:n.82+701C>T
ENST00000514217.5:c.82+701C>T	ENSP00000427688.1:n.82+701C>T
ENST00000515665.1:c.82+701C>T	ENSP00000425538.1:n.82+701C>T
NM_002185.3:c.82+701C>T	NP_002176.2:n.82+701C>T
NR_120485.1:n.185+701C>T
XM_005248299.2:c.82+701C>T	XP_005248356.1:n.82+701C>T
XM_005248300.1:c.82+701C>T	XP_005248357.1:n.82+701C>T
XM_011514037.1:c.82+701C>T	XP_011512339.1:n.82+701C>T
NM_002185.4:c.82+701C>T	NP_002176.2:n.82+701C>T
NR_120485.2:n.211+701C>T
XM_005248299.4:c.82+701C>T	XP_005248356.1:n.82+701C>T
XR_001742635.1:n.1533+1107G>A
NM_002185.5:c.82+701C>T MANE Select	NP_002176.2:n.82+701C>T
NR_120485.3:n.169+701C>T