Canonical Allele Identifier: CA359427888

Gene: IL7R

Linked Data

• gnomAD v4: 5-35867351-A-C
• MyVariant Identifiers: chr5:g.35867453A>C (hg19) ; chr5:g.35867351A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867351A>C , CM000667.2:g.35867351A>C	GRCh38
NC_000005.9:g.35867453A>C , CM000667.1:g.35867453A>C	GRCh37
NC_000005.8:g.35903210A>C	NCBI36
NG_009567.1:g.15463A>C , LRG_74:g.15463A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.267A>C MANE Select	ENSP00000306157.3:p.Gln89His
ENST00000303115.7:c.267A>C	ENSP00000306157.3:p.Gln89His
ENST00000506850.5:c.267A>C	ENSP00000421207.1:p.Gln89His
ENST00000511031.1:n.401A>C
ENST00000511982.1:c.267A>C	ENSP00000425309.1:p.Gln89His
ENST00000514217.5:c.267A>C	ENSP00000427688.1:p.Gln89His
NM_002185.3:c.267A>C	NP_002176.2:p.Gln89His
NR_120485.1:n.370A>C
XM_005248299.2:c.267A>C	XP_005248356.1:p.Gln89His
XM_005248300.1:c.267A>C	XP_005248357.1:p.Gln89His
XM_011514037.1:c.267A>C	XP_011512339.1:p.Gln89His
NM_002185.4:c.267A>C	NP_002176.2:p.Gln89His
NR_120485.2:n.396A>C
XM_005248299.4:c.267A>C	XP_005248356.1:p.Gln89His
NM_002185.5:c.267A>C MANE Select	NP_002176.2:p.Gln89His
NR_120485.3:n.354A>C