Canonical Allele Identifier: CA443891897

Gene: IL7R

Linked Data

• ClinVar Variation Id: 2967394
• ClinVar RCV Id: RCV003824072
• dbSNP Id: rs2149903309
• MyVariant Identifiers: chr5:g.35873606C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873504C>T , CM000667.2:g.35873504C>T	GRCh38
NC_000005.9:g.35873606C>T , CM000667.1:g.35873606C>T	GRCh37
NC_000005.8:g.35909363C>T	NCBI36
NG_009567.1:g.21616C>T , LRG_74:g.21616C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.562C>T MANE Select	ENSP00000306157.3:p.Leu188=
ENST00000303115.7:c.562C>T	ENSP00000306157.3:p.Leu188=
ENST00000506850.5:c.562C>T	ENSP00000421207.1:p.Leu188=
ENST00000509668.1:n.304C>T
ENST00000514217.5:c.538-2008C>T	ENSP00000427688.1:n.538-2008C>T
NM_002185.3:c.562C>T	NP_002176.2:p.Leu188=
NR_120485.1:n.641-2008C>T
XM_005248299.2:c.562C>T	XP_005248356.1:p.Leu188=
XM_005248300.1:c.562C>T	XP_005248357.1:p.Leu188=
XM_011514037.1:c.562C>T	XP_011512339.1:p.Leu188=
NM_002185.4:c.562C>T	NP_002176.2:p.Leu188=
NR_120485.2:n.667-2008C>T
XM_005248299.4:c.562C>T	XP_005248356.1:p.Leu188=
NM_002185.5:c.562C>T MANE Select	NP_002176.2:p.Leu188=
NR_120485.3:n.625-2008C>T