Canonical Allele Identifier: CA359428618

Gene: IL7R

Linked Data

• gnomAD v4: 5-35867446-T-C
• MyVariant Identifiers: chr5:g.35867548T>C (hg19) ; chr5:g.35867446T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867446T>C , CM000667.2:g.35867446T>C	GRCh38
NC_000005.9:g.35867548T>C , CM000667.1:g.35867548T>C	GRCh37
NC_000005.8:g.35903305T>C	NCBI36
NG_009567.1:g.15558T>C , LRG_74:g.15558T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.362T>C MANE Select	ENSP00000306157.3:p.Ile121Thr
ENST00000303115.7:c.362T>C	ENSP00000306157.3:p.Ile121Thr
ENST00000506850.5:c.362T>C	ENSP00000421207.1:p.Ile121Thr
ENST00000511031.1:n.496T>C
ENST00000511982.1:c.362T>C	ENSP00000425309.1:p.Ile121Thr
ENST00000514217.5:c.362T>C	ENSP00000427688.1:p.Ile121Thr
NM_002185.3:c.362T>C	NP_002176.2:p.Ile121Thr
NR_120485.1:n.465T>C
XM_005248299.2:c.362T>C	XP_005248356.1:p.Ile121Thr
XM_005248300.1:c.362T>C	XP_005248357.1:p.Ile121Thr
XM_011514037.1:c.362T>C	XP_011512339.1:p.Ile121Thr
NM_002185.4:c.362T>C	NP_002176.2:p.Ile121Thr
NR_120485.2:n.491T>C
XM_005248299.4:c.362T>C	XP_005248356.1:p.Ile121Thr
NM_002185.5:c.362T>C MANE Select	NP_002176.2:p.Ile121Thr
NR_120485.3:n.449T>C