Canonical Allele Identifier: CA444093338

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35867558C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867456C>T , CM000667.2:g.35867456C>T	GRCh38
NC_000005.9:g.35867558C>T , CM000667.1:g.35867558C>T	GRCh37
NC_000005.8:g.35903315C>T	NCBI36
NG_009567.1:g.15568C>T , LRG_74:g.15568C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.372C>T MANE Select	ENSP00000306157.3:p.Thr124=
ENST00000303115.7:c.372C>T	ENSP00000306157.3:p.Thr124=
ENST00000506850.5:c.372C>T	ENSP00000421207.1:p.Thr124=
ENST00000511031.1:n.506C>T
ENST00000511982.1:c.372C>T	ENSP00000425309.1:p.Thr124=
ENST00000514217.5:c.372C>T	ENSP00000427688.1:p.Thr124=
NM_002185.3:c.372C>T	NP_002176.2:p.Thr124=
NR_120485.1:n.475C>T
XM_005248299.2:c.372C>T	XP_005248356.1:p.Thr124=
XM_005248300.1:c.372C>T	XP_005248357.1:p.Thr124=
XM_011514037.1:c.372C>T	XP_011512339.1:p.Thr124=
NM_002185.4:c.372C>T	NP_002176.2:p.Thr124=
NR_120485.2:n.501C>T
XM_005248299.4:c.372C>T	XP_005248356.1:p.Thr124=
NM_002185.5:c.372C>T MANE Select	NP_002176.2:p.Thr124=
NR_120485.3:n.459C>T