Canonical Allele Identifier: CA558994906

Gene: IL7R

Linked Data

• dbSNP Id: rs1260306020
• gnomAD v2: 5-35857877-T-C
• gnomAD v3: 5-35857775-T-C
• gnomAD v4: 5-35857775-T-C
• MyVariant Identifiers: chr5:g.35857877T>C (hg19) ; chr5:g.35857775T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35857775T>C , CM000667.2:g.35857775T>C	GRCh38
NC_000005.9:g.35857877T>C , CM000667.1:g.35857877T>C	GRCh37
NC_000005.8:g.35893634T>C	NCBI36
NG_009567.1:g.5887T>C , LRG_74:g.5887T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.82+716T>C MANE Select	ENSP00000306157.3:n.82+716T>C
ENST00000303115.7:c.82+716T>C	ENSP00000306157.3:n.82+716T>C
ENST00000506850.5:c.82+716T>C	ENSP00000421207.1:n.82+716T>C
ENST00000508941.5:c.82+716T>C	ENSP00000426426.1:n.82+716T>C
ENST00000511031.1:n.217-3077T>C
ENST00000511982.1:c.82+716T>C	ENSP00000425309.1:n.82+716T>C
ENST00000514217.5:c.82+716T>C	ENSP00000427688.1:n.82+716T>C
ENST00000515665.1:c.82+716T>C	ENSP00000425538.1:n.82+716T>C
NM_002185.3:c.82+716T>C	NP_002176.2:n.82+716T>C
NR_120485.1:n.185+716T>C
XM_005248299.2:c.82+716T>C	XP_005248356.1:n.82+716T>C
XM_005248300.1:c.82+716T>C	XP_005248357.1:n.82+716T>C
XM_011514037.1:c.82+716T>C	XP_011512339.1:n.82+716T>C
NM_002185.4:c.82+716T>C	NP_002176.2:n.82+716T>C
NR_120485.2:n.211+716T>C
XM_005248299.4:c.82+716T>C	XP_005248356.1:n.82+716T>C
XR_001742635.1:n.1533+1092A>G
NM_002185.5:c.82+716T>C MANE Select	NP_002176.2:n.82+716T>C
NR_120485.3:n.169+716T>C