Canonical Allele Identifier: CA359430996

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35873705A>G (hg19) ; chr5:g.35873603A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873603A>G , CM000667.2:g.35873603A>G	GRCh38
NC_000005.9:g.35873705A>G , CM000667.1:g.35873705A>G	GRCh37
NC_000005.8:g.35909462A>G	NCBI36
NG_009567.1:g.21715A>G , LRG_74:g.21715A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.661A>G MANE Select	ENSP00000306157.3:p.Ser221Gly
ENST00000303115.7:c.661A>G	ENSP00000306157.3:p.Ser221Gly
ENST00000505093.1:c.70A>G	ENSP00000426069.1:p.Ser24Gly
ENST00000506850.5:c.661A>G	ENSP00000421207.1:p.Ser221Gly
ENST00000509668.1:n.403A>G
ENST00000514217.5:c.538-1909A>G	ENSP00000427688.1:n.538-1909A>G
NM_002185.3:c.661A>G	NP_002176.2:p.Ser221Gly
NR_120485.1:n.641-1909A>G
XM_005248299.2:c.661A>G	XP_005248356.1:p.Ser221Gly
XM_005248300.1:c.661A>G	XP_005248357.1:p.Ser221Gly
XM_011514037.1:c.661A>G	XP_011512339.1:p.Ser221Gly
NM_002185.4:c.661A>G	NP_002176.2:p.Ser221Gly
NR_120485.2:n.667-1909A>G
XM_005248299.4:c.661A>G	XP_005248356.1:p.Ser221Gly
NM_002185.5:c.661A>G MANE Select	NP_002176.2:p.Ser221Gly
NR_120485.3:n.625-1909A>G