Canonical Allele Identifier: CA443891891

Gene: IL7R

Linked Data

• MyVariant Identifiers: chr5:g.35873596C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35873494C>A , CM000667.2:g.35873494C>A	GRCh38
NC_000005.9:g.35873596C>A , CM000667.1:g.35873596C>A	GRCh37
NC_000005.8:g.35909353C>A	NCBI36
NG_009567.1:g.21606C>A , LRG_74:g.21606C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000303115.8:c.552C>A MANE Select	ENSP00000306157.3:p.Ser184=
ENST00000303115.7:c.552C>A	ENSP00000306157.3:p.Ser184=
ENST00000506850.5:c.552C>A	ENSP00000421207.1:p.Ser184=
ENST00000509668.1:n.294C>A
ENST00000514217.5:c.538-2018C>A	ENSP00000427688.1:n.538-2018C>A
NM_002185.3:c.552C>A	NP_002176.2:p.Ser184=
NR_120485.1:n.641-2018C>A
XM_005248299.2:c.552C>A	XP_005248356.1:p.Ser184=
XM_005248300.1:c.552C>A	XP_005248357.1:p.Ser184=
XM_011514037.1:c.552C>A	XP_011512339.1:p.Ser184=
NM_002185.4:c.552C>A	NP_002176.2:p.Ser184=
NR_120485.2:n.667-2018C>A
XM_005248299.4:c.552C>A	XP_005248356.1:p.Ser184=
NM_002185.5:c.552C>A MANE Select	NP_002176.2:p.Ser184=
NR_120485.3:n.625-2018C>A