Canonical Allele Identifier: CA305193104

Gene: TYK2

Linked Data

• dbSNP Id: rs937672335
• MyVariant Identifiers: chr19:g.10352736A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352736A>C , CM000681.2:g.10352736A>C	GRCh38
NC_000019.9:g.10463412A>C , CM000681.1:g.10463412A>C	GRCh37
NC_000019.8:g.10324412A>C	NCBI36
NG_007872.1:g.32837T>G , LRG_121:g.32837T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1550-185T>G	ENSP00000514307.1:n.*1550-185T>G
ENST00000525976.6:c.3201-185T>G	ENSP00000434831.2:n.3201-185T>G
ENST00000527481.3:c.3082-185T>G	ENSP00000466340.2:n.3082-185T>G
ENST00000529370.6:n.4577-185T>G
ENST00000529739.2:n.4010-185T>G
ENST00000530829.2:c.*2752-185T>G	ENSP00000436826.2:n.*2752-185T>G
ENST00000531836.6:c.3201-185T>G	ENSP00000436175.2:n.3201-185T>G
ENST00000533334.2:c.*1242+190T>G	ENSP00000432320.2:n.*1242+190T>G
ENST00000534228.2:n.5054+190T>G
ENST00000699354.1:n.1303-185T>G
ENST00000699355.1:c.*2701-185T>G	ENSP00000514328.1:n.*2701-185T>G
ENST00000699356.1:n.4010-185T>G
ENST00000699357.1:n.5055-185T>G
ENST00000699358.1:c.3200+190T>G	ENSP00000514329.1:n.3200+190T>G
ENST00000699359.1:c.375-185T>G
ENST00000699360.1:c.3159-185T>G	ENSP00000514331.1:n.3159-185T>G
ENST00000699361.1:n.50T>G
ENST00000699362.1:c.97-185T>G	ENSP00000514332.1:n.97-185T>G
ENST00000699363.1:c.97-185T>G	ENSP00000514333.1:n.97-185T>G
ENST00000699364.1:n.201-185T>G
ENST00000699365.1:c.270-185T>G	ENSP00000514334.1:n.270-185T>G
ENST00000699366.1:n.111+1078T>G
ENST00000699367.1:n.111+1078T>G
ENST00000699368.1:c.688-185T>G	ENSP00000514335.1:n.688-185T>G
ENST00000525621.6:c.3201-185T>G MANE Select	ENSP00000431885.1:n.3201-185T>G
ENST00000264818.10:c.3201-185T>G	ENSP00000264818.6:n.3201-185T>G
ENST00000524462.5:c.2646-185T>G	ENSP00000433203.1:n.2646-185T>G
ENST00000525621.5:c.3201-185T>G	ENSP00000431885.1:n.3201-185T>G
ENST00000527481.2:c.378-185T>G
ENST00000529422.1:n.116+286T>G
ENST00000529739.1:c.270-185T>G	ENSP00000436155.1:n.270-185T>G
ENST00000530220.1:n.331+190T>G
ENST00000530560.5:c.337+1306T>G	ENSP00000465291.1:n.337+1306T>G
ENST00000592137.1:n.355-185T>G
NM_003331.4:c.3201-185T>G , LRG_121t1:c.3201-185T>G	NP_003322.3:n.3201-185T>G
XM_011528245.1:c.3201-185T>G	XP_011526547.1:n.3201-185T>G
XM_011528246.1:c.2904-185T>G	XP_011526548.1:n.2904-185T>G
XM_011528247.1:c.2904-185T>G	XP_011526549.1:n.2904-185T>G
XM_011528248.1:c.3200+190T>G	XP_011526550.1:n.3200+190T>G
XM_011528249.1:c.1875-185T>G	XP_011526551.1:n.1875-185T>G
XM_011528251.1:c.1458-185T>G	XP_011526553.1:n.1458-185T>G
XM_011528246.3:c.2904-185T>G	XP_011526548.1:n.2904-185T>G
XM_011528249.2:c.1875-185T>G	XP_011526551.1:n.1875-185T>G
XR_001753750.1:n.3357+190T>G
XR_001753751.1:n.3753-185T>G
XR_002958353.1:n.4679-185T>G
NM_003331.5:c.3201-185T>G MANE Select	NP_003322.3:n.3201-185T>G
NM_001385197.1:c.3201-185T>G	NP_001372126.1:n.3201-185T>G
NM_001385198.1:c.3168+222T>G	NP_001372127.1:n.3168+222T>G
NM_001385199.1:c.3015-185T>G	NP_001372128.1:n.3015-185T>G
NM_001385200.1:c.3198-185T>G	NP_001372129.1:n.3198-185T>G
NM_001385201.1:c.3003-185T>G	NP_001372130.1:n.3003-185T>G
NM_001385202.1:c.3117-185T>G	NP_001372131.1:n.3117-185T>G
NM_001385203.1:c.3282-185T>G	NP_001372132.1:n.3282-185T>G
NM_001385204.1:c.3411-185T>G	NP_001372133.1:n.3411-185T>G
NM_001385205.1:c.3111-185T>G	NP_001372134.1:n.3111-185T>G
NM_001385206.1:c.3075-185T>G	NP_001372135.1:n.3075-185T>G
NM_001385207.1:c.3183-185T>G	NP_001372136.1:n.3183-185T>G