Canonical Allele Identifier: CA359431013

Gene: IL7R

Linked Data

• dbSNP Id: rs1394251315
• MyVariant Identifiers: chr5:g.35873708C>G (hg19) ; chr5:g.35873606C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873606C>G , CM000667.2:g.35873606C>G	GRCh38
NC_000005.9:g.35873708C>G , CM000667.1:g.35873708C>G	GRCh37
NC_000005.8:g.35909465C>G	NCBI36
NG_009567.1:g.21718C>G , LRG_74:g.21718C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.664C>G MANE Select	ENSP00000306157.3:p.Pro222Ala
ENST00000303115.7:c.664C>G	ENSP00000306157.3:p.Pro222Ala
ENST00000505093.1:c.73C>G	ENSP00000426069.1:p.Pro25Ala
ENST00000506850.5:c.664C>G	ENSP00000421207.1:p.Pro222Ala
ENST00000509668.1:n.406C>G
ENST00000514217.5:c.538-1906C>G	ENSP00000427688.1:n.538-1906C>G
NM_002185.3:c.664C>G	NP_002176.2:p.Pro222Ala
NR_120485.1:n.641-1906C>G
XM_005248299.2:c.664C>G	XP_005248356.1:p.Pro222Ala
XM_005248300.1:c.664C>G	XP_005248357.1:p.Pro222Ala
XM_011514037.1:c.664C>G	XP_011512339.1:p.Pro222Ala
NM_002185.4:c.664C>G	NP_002176.2:p.Pro222Ala
NR_120485.2:n.667-1906C>G
XM_005248299.4:c.664C>G	XP_005248356.1:p.Pro222Ala
NM_002185.5:c.664C>G MANE Select	NP_002176.2:p.Pro222Ala
NR_120485.3:n.625-1906C>G