Canonical Allele Identifier: CA505476436

Gene: TYK2

Linked Data

• dbSNP Id: rs1453957454
• gnomAD v3: 19-10357911-C-T
• gnomAD v4: 19-10357911-C-T
• MyVariant Identifiers: chr19:g.10468587C>T (hg19) ; chr19:g.10357911C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357911C>T , CM000681.2:g.10357911C>T	GRCh38
NC_000019.9:g.10468587C>T , CM000681.1:g.10468587C>T	GRCh37
NC_000019.8:g.10329587C>T	NCBI36
NG_007872.1:g.27662G>A , LRG_121:g.27662G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*668G>A	ENSP00000514307.1:n.*668G>A
ENST00000525976.6:c.2319G>A	ENSP00000434831.2:p.Val773=
ENST00000527481.3:c.2319G>A	ENSP00000466340.2:p.Val773=
ENST00000529370.6:n.2650G>A
ENST00000529739.2:n.2733G>A
ENST00000530829.2:c.*1870G>A	ENSP00000436826.2:n.*1870G>A
ENST00000531836.6:c.2319G>A	ENSP00000436175.2:p.Val773=
ENST00000533334.2:c.*361G>A	ENSP00000432320.2:n.*361G>A
ENST00000534228.2:n.2733G>A
ENST00000699354.1:n.421G>A
ENST00000699355.1:c.*379G>A	ENSP00000514328.1:n.*379G>A
ENST00000699356.1:n.2733G>A
ENST00000699357.1:n.2733G>A
ENST00000699358.1:c.2319G>A	ENSP00000514329.1:p.Val773=
ENST00000699360.1:c.2319G>A	ENSP00000514331.1:p.Val773=
ENST00000525621.6:c.2319G>A MANE Select	ENSP00000431885.1:p.Val773=
ENST00000264818.10:c.2319G>A	ENSP00000264818.6:p.Val773=
ENST00000524462.5:c.1764G>A	ENSP00000433203.1:p.Val588=
ENST00000525621.5:c.2319G>A	ENSP00000431885.1:p.Val773=
ENST00000529370.5:c.2319G>A	ENSP00000432728.1:p.Val773=
ENST00000533334.1:c.608G>A
NM_003331.4:c.2319G>A , LRG_121t1:c.2319G>A	NP_003322.3:p.Val773=
XM_011528245.1:c.2319G>A	XP_011526547.1:p.Val773=
XM_011528246.1:c.2022G>A	XP_011526548.1:p.Val674=
XM_011528247.1:c.2022G>A	XP_011526549.1:p.Val674=
XM_011528248.1:c.2319G>A	XP_011526550.1:p.Val773=
XM_011528249.1:c.993G>A	XP_011526551.1:p.Val331=
XM_011528251.1:c.576G>A	XP_011526553.1:p.Val192=
XM_011528246.3:c.2022G>A	XP_011526548.1:p.Val674=
XM_011528249.2:c.993G>A	XP_011526551.1:p.Val331=
XR_001753750.1:n.2476G>A
XR_001753751.1:n.2476G>A
XR_001753752.1:n.2588G>A
XR_002958353.1:n.2357G>A
NM_003331.5:c.2319G>A MANE Select	NP_003322.3:p.Val773=
NM_001385197.1:c.2319G>A	NP_001372126.1:p.Val773=
NM_001385198.1:c.2319G>A	NP_001372127.1:p.Val773=
NM_001385199.1:c.2133G>A	NP_001372128.1:p.Val711=
NM_001385200.1:c.2319G>A	NP_001372129.1:p.Val773=
NM_001385201.1:c.2121G>A	NP_001372130.1:p.Val707=
NM_001385202.1:c.2235G>A	NP_001372131.1:p.Val745=
NM_001385203.1:c.2319G>A	NP_001372132.1:p.Val773=
NM_001385204.1:c.2319G>A	NP_001372133.1:p.Val773=
NM_001385205.1:c.2229G>A	NP_001372134.1:p.Val743=
NM_001385206.1:c.2193G>A	NP_001372135.1:p.Val731=
NM_001385207.1:c.2301G>A	NP_001372136.1:p.Val767=