Canonical Allele Identifier: CA359430955

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35873698T>G (hg19) ; chr5:g.35873596T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873596T>G , CM000667.2:g.35873596T>G	GRCh38
NC_000005.9:g.35873698T>G , CM000667.1:g.35873698T>G	GRCh37
NC_000005.8:g.35909455T>G	NCBI36
NG_009567.1:g.21708T>G , LRG_74:g.21708T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.654T>G MANE Select	ENSP00000306157.3:p.Ser218Arg
ENST00000303115.7:c.654T>G	ENSP00000306157.3:p.Ser218Arg
ENST00000505093.1:c.63T>G	ENSP00000426069.1:p.Ser21Arg
ENST00000506850.5:c.654T>G	ENSP00000421207.1:p.Ser218Arg
ENST00000509668.1:n.396T>G
ENST00000514217.5:c.538-1916T>G	ENSP00000427688.1:n.538-1916T>G
NM_002185.3:c.654T>G	NP_002176.2:p.Ser218Arg
NR_120485.1:n.641-1916T>G
XM_005248299.2:c.654T>G	XP_005248356.1:p.Ser218Arg
XM_005248300.1:c.654T>G	XP_005248357.1:p.Ser218Arg
XM_011514037.1:c.654T>G	XP_011512339.1:p.Ser218Arg
NM_002185.4:c.654T>G	NP_002176.2:p.Ser218Arg
NR_120485.2:n.667-1916T>G
XM_005248299.4:c.654T>G	XP_005248356.1:p.Ser218Arg
NM_002185.5:c.654T>G MANE Select	NP_002176.2:p.Ser218Arg
NR_120485.3:n.625-1916T>G