Canonical Allele Identifier: CA305192460

Gene: TYK2

Linked Data

• dbSNP Id: rs1003106473
• gnomAD v3: 19-10352189-A-G
• gnomAD v4: 19-10352189-A-G
• MyVariant Identifiers: chr19:g.10462865A>G (hg19) ; chr19:g.10352189A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352189A>G , CM000681.2:g.10352189A>G	GRCh38
NC_000019.9:g.10462865A>G , CM000681.1:g.10462865A>G	GRCh37
NC_000019.8:g.10323865A>G	NCBI36
NG_007872.1:g.33384T>C , LRG_121:g.33384T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1667+245T>C	ENSP00000514307.1:n.*1667+245T>C
ENST00000525976.6:c.3318+245T>C	ENSP00000434831.2:n.3318+245T>C
ENST00000527481.3:c.*88+245T>C	ENSP00000466340.2:n.*88+245T>C
ENST00000529370.6:n.4694+245T>C
ENST00000529739.2:n.4127+245T>C
ENST00000530829.2:c.*2869+245T>C	ENSP00000436826.2:n.*2869+245T>C
ENST00000531836.6:c.3318+245T>C	ENSP00000436175.2:n.3318+245T>C
ENST00000533334.2:c.*1242+737T>C	ENSP00000432320.2:n.*1242+737T>C
ENST00000534228.2:n.5054+737T>C
ENST00000699354.1:n.1420+245T>C
ENST00000699355.1:c.*2818+245T>C	ENSP00000514328.1:n.*2818+245T>C
ENST00000699356.1:n.4127+245T>C
ENST00000699357.1:n.5172+245T>C
ENST00000699358.1:c.3200+737T>C	ENSP00000514329.1:n.3200+737T>C
ENST00000699359.1:c.492+245T>C
ENST00000699360.1:c.3276+245T>C	ENSP00000514331.1:n.3276+245T>C
ENST00000699361.1:n.352+245T>C
ENST00000699362.1:c.214+245T>C	ENSP00000514332.1:n.214+245T>C
ENST00000699363.1:c.214+245T>C	ENSP00000514333.1:n.214+245T>C
ENST00000699364.1:n.318+245T>C
ENST00000699365.1:c.387+245T>C	ENSP00000514334.1:n.387+245T>C
ENST00000699366.1:n.112-1221T>C
ENST00000699367.1:n.112-1027T>C
ENST00000699368.1:c.805+245T>C	ENSP00000514335.1:n.805+245T>C
ENST00000525621.6:c.3318+245T>C MANE Select	ENSP00000431885.1:n.3318+245T>C
ENST00000264818.10:c.3318+245T>C	ENSP00000264818.6:n.3318+245T>C
ENST00000524462.5:c.2763+245T>C	ENSP00000433203.1:n.2763+245T>C
ENST00000525621.5:c.3318+245T>C	ENSP00000431885.1:n.3318+245T>C
ENST00000525976.5:c.59+245T>C
ENST00000527481.2:c.495+245T>C
ENST00000529422.1:n.116+833T>C
ENST00000530220.1:n.331+737T>C
ENST00000530560.5:c.338-1221T>C	ENSP00000465291.1:n.338-1221T>C
ENST00000592137.1:n.472+245T>C
NM_003331.4:c.3318+245T>C , LRG_121t1:c.3318+245T>C	NP_003322.3:n.3318+245T>C
XM_011528245.1:c.3318+245T>C	XP_011526547.1:n.3318+245T>C
XM_011528246.1:c.3021+245T>C	XP_011526548.1:n.3021+245T>C
XM_011528247.1:c.3021+245T>C	XP_011526549.1:n.3021+245T>C
XM_011528248.1:c.3200+737T>C	XP_011526550.1:n.3200+737T>C
XM_011528249.1:c.1992+245T>C	XP_011526551.1:n.1992+245T>C
XM_011528251.1:c.1575+245T>C	XP_011526553.1:n.1575+245T>C
XM_011528246.3:c.3021+245T>C	XP_011526548.1:n.3021+245T>C
XM_011528249.2:c.1992+245T>C	XP_011526551.1:n.1992+245T>C
XR_001753750.1:n.3357+737T>C
XR_001753751.1:n.3870+245T>C
XR_002958353.1:n.4796+245T>C
NM_003331.5:c.3318+245T>C MANE Select	NP_003322.3:n.3318+245T>C
NM_001385197.1:c.3318+245T>C	NP_001372126.1:n.3318+245T>C
NM_001385198.1:c.3168+769T>C	NP_001372127.1:n.3168+769T>C
NM_001385199.1:c.3132+245T>C	NP_001372128.1:n.3132+245T>C
NM_001385200.1:c.3315+245T>C	NP_001372129.1:n.3315+245T>C
NM_001385201.1:c.3120+245T>C	NP_001372130.1:n.3120+245T>C
NM_001385202.1:c.3234+245T>C	NP_001372131.1:n.3234+245T>C
NM_001385203.1:c.3399+245T>C	NP_001372132.1:n.3399+245T>C
NM_001385204.1:c.3528+245T>C	NP_001372133.1:n.3528+245T>C
NM_001385205.1:c.3228+245T>C	NP_001372134.1:n.3228+245T>C
NM_001385206.1:c.3192+245T>C	NP_001372135.1:n.3192+245T>C
NM_001385207.1:c.3300+245T>C	NP_001372136.1:n.3300+245T>C