Canonical Allele Identifier: CA1539052315
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35873517A= , CM000667.2:g.35873517A= GRCh38
NC_000005.9:g.35873619A= , CM000667.1:g.35873619A= GRCh37
NC_000005.8:g.35909376A= NCBI36
NG_009567.1:g.21629A= , LRG_74:g.21629A=

Transcript Alleles

HGVS Amino-acid change
ENST00000303115.8:c.575A= MANE Select ENSP00000306157.3:p.Gln192=
ENST00000303115.7:c.575A= ENSP00000306157.3:p.Gln192=
ENST00000506850.5:c.575A= ENSP00000421207.1:p.Gln192=
ENST00000509668.1:n.317A=
ENST00000514217.5:c.538-1995A= ENSP00000427688.1:n.538-1995A=
NM_002185.3:c.575A= NP_002176.2:p.Gln192=
NR_120485.1:n.641-1995A=
XM_005248299.2:c.575A= XP_005248356.1:p.Gln192=
XM_005248300.1:c.575A= XP_005248357.1:p.Gln192=
XM_011514037.1:c.575A= XP_011512339.1:p.Gln192=
NM_002185.4:c.575A= NP_002176.2:p.Gln192=
NR_120485.2:n.667-1995A=
XM_005248299.4:c.575A= XP_005248356.1:p.Gln192=
NM_002185.5:c.575A= MANE Select NP_002176.2:p.Gln192=
NR_120485.3:n.625-1995A=