Canonical Allele Identifier: CA444093258

Gene: IL7R

Linked Data

• gnomAD v4: 5-35867381-C-T
• COSMIC: COSM3615739
• MyVariant Identifiers: chr5:g.35867483C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35867381C>T , CM000667.2:g.35867381C>T	GRCh38
NC_000005.9:g.35867483C>T , CM000667.1:g.35867483C>T	GRCh37
NC_000005.8:g.35903240C>T	NCBI36
NG_009567.1:g.15493C>T , LRG_74:g.15493C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303115.8:c.297C>T MANE Select	ENSP00000306157.3:p.Phe99=
ENST00000303115.7:c.297C>T	ENSP00000306157.3:p.Phe99=
ENST00000506850.5:c.297C>T	ENSP00000421207.1:p.Phe99=
ENST00000511031.1:n.431C>T
ENST00000511982.1:c.297C>T	ENSP00000425309.1:p.Phe99=
ENST00000514217.5:c.297C>T	ENSP00000427688.1:p.Phe99=
NM_002185.3:c.297C>T	NP_002176.2:p.Phe99=
NR_120485.1:n.400C>T
XM_005248299.2:c.297C>T	XP_005248356.1:p.Phe99=
XM_005248300.1:c.297C>T	XP_005248357.1:p.Phe99=
XM_011514037.1:c.297C>T	XP_011512339.1:p.Phe99=
NM_002185.4:c.297C>T	NP_002176.2:p.Phe99=
NR_120485.2:n.426C>T
XM_005248299.4:c.297C>T	XP_005248356.1:p.Phe99=
NM_002185.5:c.297C>T MANE Select	NP_002176.2:p.Phe99=
NR_120485.3:n.384C>T