Canonical Allele Identifier: CA3231919

Gene: IL7R

Linked Data

• dbSNP Id: rs778262602
• ExAC: 5:35867521 G / T
• gnomAD v2: 5-35867521-G-T
• gnomAD v3: 5-35867419-G-T
• gnomAD v4: 5-35867419-G-T
• MyVariant Identifiers: chr5:g.35867521G>T (hg19) ; chr5:g.35867419G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867419G>T , CM000667.2:g.35867419G>T	GRCh38
NC_000005.9:g.35867521G>T , CM000667.1:g.35867521G>T	GRCh37
NC_000005.8:g.35903278G>T	NCBI36
NG_009567.1:g.15531G>T , LRG_74:g.15531G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.335G>T MANE Select	ENSP00000306157.3:p.Gly112Val
ENST00000303115.7:c.335G>T	ENSP00000306157.3:p.Gly112Val
ENST00000506850.5:c.335G>T	ENSP00000421207.1:p.Gly112Val
ENST00000511031.1:n.469G>T
ENST00000511982.1:c.335G>T	ENSP00000425309.1:p.Gly112Val
ENST00000514217.5:c.335G>T	ENSP00000427688.1:p.Gly112Val
NM_002185.3:c.335G>T	NP_002176.2:p.Gly112Val
NR_120485.1:n.438G>T
XM_005248299.2:c.335G>T	XP_005248356.1:p.Gly112Val
XM_005248300.1:c.335G>T	XP_005248357.1:p.Gly112Val
XM_011514037.1:c.335G>T	XP_011512339.1:p.Gly112Val
NM_002185.4:c.335G>T	NP_002176.2:p.Gly112Val
NR_120485.2:n.464G>T
XM_005248299.4:c.335G>T	XP_005248356.1:p.Gly112Val
NM_002185.5:c.335G>T MANE Select	NP_002176.2:p.Gly112Val
NR_120485.3:n.422G>T