Canonical Allele Identifier: CA359430574

Gene: IL7R

Linked Data

• gnomAD v4: 5-35873498-A-G
• MyVariant Identifiers: chr5:g.35873600A>G (hg19) ; chr5:g.35873498A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873498A>G , CM000667.2:g.35873498A>G	GRCh38
NC_000005.9:g.35873600A>G , CM000667.1:g.35873600A>G	GRCh37
NC_000005.8:g.35909357A>G	NCBI36
NG_009567.1:g.21610A>G , LRG_74:g.21610A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.556A>G MANE Select	ENSP00000306157.3:p.Thr186Ala
ENST00000303115.7:c.556A>G	ENSP00000306157.3:p.Thr186Ala
ENST00000506850.5:c.556A>G	ENSP00000421207.1:p.Thr186Ala
ENST00000509668.1:n.298A>G
ENST00000514217.5:c.538-2014A>G	ENSP00000427688.1:n.538-2014A>G
NM_002185.3:c.556A>G	NP_002176.2:p.Thr186Ala
NR_120485.1:n.641-2014A>G
XM_005248299.2:c.556A>G	XP_005248356.1:p.Thr186Ala
XM_005248300.1:c.556A>G	XP_005248357.1:p.Thr186Ala
XM_011514037.1:c.556A>G	XP_011512339.1:p.Thr186Ala
NM_002185.4:c.556A>G	NP_002176.2:p.Thr186Ala
NR_120485.2:n.667-2014A>G
XM_005248299.4:c.556A>G	XP_005248356.1:p.Thr186Ala
NM_002185.5:c.556A>G MANE Select	NP_002176.2:p.Thr186Ala
NR_120485.3:n.625-2014A>G