Canonical Allele Identifier: CA214058

Gene: IL7R

Linked Data

• ClinVar Variation Id: 36397
• ClinVar RCV Id: RCV000030066
• dbSNP Id: rs193922646
• MyVariant Identifiers: chr5:g.35860936A>G (hg19) ; chr5:g.35860834A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35860834A>G , CM000667.2:g.35860834A>G	GRCh38
NC_000005.9:g.35860936A>G , CM000667.1:g.35860936A>G	GRCh37
NC_000005.8:g.35896693A>G	NCBI36
NG_009567.1:g.8946A>G , LRG_74:g.8946A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.83-18A>G MANE Select	ENSP00000306157.3:n.83-18A>G
ENST00000303115.7:c.83-18A>G	ENSP00000306157.3:n.83-18A>G
ENST00000506850.5:c.83-18A>G	ENSP00000421207.1:n.83-18A>G
ENST00000508941.5:c.83-18A>G	ENSP00000426426.1:n.83-18A>G
ENST00000511031.1:n.217-18A>G
ENST00000511982.1:c.83-18A>G	ENSP00000425309.1:n.83-18A>G
ENST00000514217.5:c.83-18A>G	ENSP00000427688.1:n.83-18A>G
ENST00000515665.1:c.83-18A>G	ENSP00000425538.1:n.83-18A>G
NM_002185.3:c.83-18A>G	NP_002176.2:n.83-18A>G
NR_120485.1:n.186-18A>G
XM_005248299.2:c.83-18A>G	XP_005248356.1:n.83-18A>G
XM_005248300.1:c.83-18A>G	XP_005248357.1:n.83-18A>G
XM_011514037.1:c.83-18A>G	XP_011512339.1:n.83-18A>G
NM_002185.4:c.83-18A>G	NP_002176.2:n.83-18A>G
NR_120485.2:n.212-18A>G
XM_005248299.4:c.83-18A>G	XP_005248356.1:n.83-18A>G
NM_002185.5:c.83-18A>G MANE Select	NP_002176.2:n.83-18A>G
NR_120485.3:n.170-18A>G