Canonical Allele Identifier: CA359430609

Gene: IL7R

Linked Data

• dbSNP Id: rs1345734622
• MyVariant Identifiers: chr5:g.35873619A>C (hg19) ; chr5:g.35873517A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.575A>C MANE Select	ENSP00000306157.3:p.Gln192Pro
ENST00000303115.7:c.575A>C	ENSP00000306157.3:p.Gln192Pro
ENST00000506850.5:c.575A>C	ENSP00000421207.1:p.Gln192Pro
ENST00000509668.1:n.317A>C
ENST00000514217.5:c.538-1995A>C	ENSP00000427688.1:n.538-1995A>C
NM_002185.3:c.575A>C	NP_002176.2:p.Gln192Pro
NR_120485.1:n.641-1995A>C
XM_005248299.2:c.575A>C	XP_005248356.1:p.Gln192Pro
XM_005248300.1:c.575A>C	XP_005248357.1:p.Gln192Pro
XM_011514037.1:c.575A>C	XP_011512339.1:p.Gln192Pro
NM_002185.4:c.575A>C	NP_002176.2:p.Gln192Pro
NR_120485.2:n.667-1995A>C
XM_005248299.4:c.575A>C	XP_005248356.1:p.Gln192Pro
NM_002185.5:c.575A>C MANE Select	NP_002176.2:p.Gln192Pro
NR_120485.3:n.625-1995A>C