Canonical Allele Identifier: CA359428645

Gene: IL7R

Linked Data

• dbSNP Id: rs1759968837
• MyVariant Identifiers: chr5:g.35867557C>A (hg19) ; chr5:g.35867455C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867455C>A , CM000667.2:g.35867455C>A	GRCh38
NC_000005.9:g.35867557C>A , CM000667.1:g.35867557C>A	GRCh37
NC_000005.8:g.35903314C>A	NCBI36
NG_009567.1:g.15567C>A , LRG_74:g.15567C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.371C>A MANE Select	ENSP00000306157.3:p.Thr124Asn
ENST00000303115.7:c.371C>A	ENSP00000306157.3:p.Thr124Asn
ENST00000506850.5:c.371C>A	ENSP00000421207.1:p.Thr124Asn
ENST00000511031.1:n.505C>A
ENST00000511982.1:c.371C>A	ENSP00000425309.1:p.Thr124Asn
ENST00000514217.5:c.371C>A	ENSP00000427688.1:p.Thr124Asn
NM_002185.3:c.371C>A	NP_002176.2:p.Thr124Asn
NR_120485.1:n.474C>A
XM_005248299.2:c.371C>A	XP_005248356.1:p.Thr124Asn
XM_005248300.1:c.371C>A	XP_005248357.1:p.Thr124Asn
XM_011514037.1:c.371C>A	XP_011512339.1:p.Thr124Asn
NM_002185.4:c.371C>A	NP_002176.2:p.Thr124Asn
NR_120485.2:n.500C>A
XM_005248299.4:c.371C>A	XP_005248356.1:p.Thr124Asn
NM_002185.5:c.371C>A MANE Select	NP_002176.2:p.Thr124Asn
NR_120485.3:n.458C>A