Canonical Allele Identifier: CA124396
Gene: IL7R HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14842
ClinVar RCV Id: RCV000015967
dbSNP Id: rs104893893

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35873593G>A , CM000667.2:g.35873593G>A GRCh38
NC_000005.9:g.35873695G>A , CM000667.1:g.35873695G>A GRCh37
NC_000005.8:g.35909452G>A NCBI36
NG_009567.1:g.21705G>A , LRG_74:g.21705G>A

Transcript Alleles

HGVS Amino-acid change
NM_002185.3:c.651G>A VV NP_002176.2:p.Trp217Ter
NR_120485.1:n.641-1919G>A
XM_005248299.2:c.651G>A XP_005248356.1:p.Trp217Ter
XM_005248300.1:c.651G>A XP_005248357.1:p.Trp217Ter
XM_011514037.1:c.651G>A XP_011512339.1:p.Trp217Ter
NM_002185.4:c.651G>A VV
NR_120485.2:n.667-1919G>A
XM_005248299.4:c.651G>A
NM_002185.5:c.651G>A VV MANE Preferred
ENST00000303115.7:c.651G>A ENSP00000306157.3:p.Trp217Ter
ENST00000505093.1:n.60G>A ENSP00000426069.1:p.Trp20Ter
ENST00000506850.5:c.651G>A ENSP00000421207.1:p.Trp217Ter
ENST00000509668.1:n.393G>A
ENST00000514217.5:c.538-1919G>A ENSP00000427688.1:p.=