Canonical Allele Identifier: CA359427940

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35867460T>G (hg19) ; chr5:g.35867358T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867358T>G , CM000667.2:g.35867358T>G	GRCh38
NC_000005.9:g.35867460T>G , CM000667.1:g.35867460T>G	GRCh37
NC_000005.8:g.35903217T>G	NCBI36
NG_009567.1:g.15470T>G , LRG_74:g.15470T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.274T>G MANE Select	ENSP00000306157.3:p.Tyr92Asp
ENST00000303115.7:c.274T>G	ENSP00000306157.3:p.Tyr92Asp
ENST00000506850.5:c.274T>G	ENSP00000421207.1:p.Tyr92Asp
ENST00000511031.1:n.408T>G
ENST00000511982.1:c.274T>G	ENSP00000425309.1:p.Tyr92Asp
ENST00000514217.5:c.274T>G	ENSP00000427688.1:p.Tyr92Asp
NM_002185.3:c.274T>G	NP_002176.2:p.Tyr92Asp
NR_120485.1:n.377T>G
XM_005248299.2:c.274T>G	XP_005248356.1:p.Tyr92Asp
XM_005248300.1:c.274T>G	XP_005248357.1:p.Tyr92Asp
XM_011514037.1:c.274T>G	XP_011512339.1:p.Tyr92Asp
NM_002185.4:c.274T>G	NP_002176.2:p.Tyr92Asp
NR_120485.2:n.403T>G
XM_005248299.4:c.274T>G	XP_005248356.1:p.Tyr92Asp
NM_002185.5:c.274T>G MANE Select	NP_002176.2:p.Tyr92Asp
NR_120485.3:n.361T>G