Canonical Allele Identifier: CA9193070

Gene: TYK2

Linked Data

• dbSNP Id: rs376243401
• ExAC: 19:10468440 C / T
• gnomAD v2: 19-10468440-C-T
• MyVariant Identifiers: chr19:g.10468440C>T (hg19) ; chr19:g.10357764C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357764C>T , CM000681.2:g.10357764C>T	GRCh38
NC_000019.9:g.10468440C>T , CM000681.1:g.10468440C>T	GRCh37
NC_000019.8:g.10329440C>T	NCBI36
NG_007872.1:g.27809G>A , LRG_121:g.27809G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*815G>A	ENSP00000514307.1:n.*815G>A
ENST00000525976.6:c.2466G>A	ENSP00000434831.2:p.Glu822=
ENST00000527481.3:c.2466G>A	ENSP00000466340.2:p.Glu822=
ENST00000529370.6:n.2797G>A
ENST00000529739.2:n.2880G>A
ENST00000530829.2:c.*2017G>A	ENSP00000436826.2:n.*2017G>A
ENST00000531836.6:c.2466G>A	ENSP00000436175.2:p.Glu822=
ENST00000533334.2:c.*508G>A	ENSP00000432320.2:n.*508G>A
ENST00000534228.2:n.2880G>A
ENST00000699354.1:n.568G>A
ENST00000699355.1:c.*526G>A	ENSP00000514328.1:n.*526G>A
ENST00000699356.1:n.2880G>A
ENST00000699357.1:n.2880G>A
ENST00000699358.1:c.2466G>A	ENSP00000514329.1:p.Glu822=
ENST00000699360.1:c.2466G>A	ENSP00000514331.1:p.Glu822=
ENST00000525621.6:c.2466G>A MANE Select	ENSP00000431885.1:p.Glu822=
ENST00000264818.10:c.2466G>A	ENSP00000264818.6:p.Glu822=
ENST00000524462.5:c.1911G>A	ENSP00000433203.1:p.Glu637=
ENST00000525621.5:c.2466G>A	ENSP00000431885.1:p.Glu822=
ENST00000529370.5:c.2466G>A	ENSP00000432728.1:p.Glu822=
ENST00000529412.1:n.138G>A
NM_003331.4:c.2466G>A , LRG_121t1:c.2466G>A	NP_003322.3:p.Glu822=
XM_011528245.1:c.2466G>A	XP_011526547.1:p.Glu822=
XM_011528246.1:c.2169G>A	XP_011526548.1:p.Glu723=
XM_011528247.1:c.2169G>A	XP_011526549.1:p.Glu723=
XM_011528248.1:c.2466G>A	XP_011526550.1:p.Glu822=
XM_011528249.1:c.1140G>A	XP_011526551.1:p.Glu380=
XM_011528251.1:c.723G>A	XP_011526553.1:p.Glu241=
XM_011528246.3:c.2169G>A	XP_011526548.1:p.Glu723=
XM_011528249.2:c.1140G>A	XP_011526551.1:p.Glu380=
XR_001753750.1:n.2623G>A
XR_001753751.1:n.2623G>A
XR_002958353.1:n.2504G>A
NM_003331.5:c.2466G>A MANE Select	NP_003322.3:p.Glu822=
NM_001385197.1:c.2466G>A	NP_001372126.1:p.Glu822=
NM_001385198.1:c.2466G>A	NP_001372127.1:p.Glu822=
NM_001385199.1:c.2280G>A	NP_001372128.1:p.Glu760=
NM_001385200.1:c.2466G>A	NP_001372129.1:p.Glu822=
NM_001385201.1:c.2268G>A	NP_001372130.1:p.Glu756=
NM_001385202.1:c.2382G>A	NP_001372131.1:p.Glu794=
NM_001385203.1:c.2466G>A	NP_001372132.1:p.Glu822=
NM_001385204.1:c.2466G>A	NP_001372133.1:p.Glu822=
NM_001385205.1:c.2376G>A	NP_001372134.1:p.Glu792=
NM_001385206.1:c.2340G>A	NP_001372135.1:p.Glu780=
NM_001385207.1:c.2448G>A	NP_001372136.1:p.Glu816=