Canonical Allele Identifier: CA305204195

Gene: TYK2

Linked Data

• dbSNP Id: rs865816160
• gnomAD v3: 19-10361883-G-A
• gnomAD v4: 19-10361883-G-A
• MyVariant Identifiers: chr19:g.10472559G>A (hg19) ; chr19:g.10361883G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10361883G>A , CM000681.2:g.10361883G>A	GRCh38
NC_000019.9:g.10472559G>A , CM000681.1:g.10472559G>A	GRCh37
NC_000019.8:g.10333559G>A	NCBI36
NG_007872.1:g.23690C>T , LRG_121:g.23690C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*195C>T	ENSP00000514307.1:n.*195C>T
ENST00000525976.6:c.1846C>T	ENSP00000434831.2:p.Pro616Ser
ENST00000527481.3:c.1846C>T	ENSP00000466340.2:p.Pro616Ser
ENST00000529370.6:n.2177C>T
ENST00000529739.2:n.2260C>T
ENST00000530829.2:c.*1397C>T	ENSP00000436826.2:n.*1397C>T
ENST00000531836.6:c.1846C>T	ENSP00000436175.2:p.Pro616Ser
ENST00000533334.2:c.1846C>T	ENSP00000432320.2:p.Pro616Ser
ENST00000534228.2:n.2260C>T
ENST00000699355.1:c.1774-47C>T	ENSP00000514328.1:n.1774-47C>T
ENST00000699356.1:n.2260C>T
ENST00000699357.1:n.2260C>T
ENST00000699358.1:c.1846C>T	ENSP00000514329.1:p.Pro616Ser
ENST00000699360.1:c.1846C>T	ENSP00000514331.1:p.Pro616Ser
ENST00000525621.6:c.1846C>T MANE Select	ENSP00000431885.1:p.Pro616Ser
ENST00000264818.10:c.1846C>T	ENSP00000264818.6:p.Pro616Ser
ENST00000524462.5:c.1291C>T	ENSP00000433203.1:p.Pro431Ser
ENST00000525621.5:c.1846C>T	ENSP00000431885.1:p.Pro616Ser
ENST00000529370.5:c.1846C>T	ENSP00000432728.1:p.Pro616Ser
ENST00000531620.1:n.179C>T
ENST00000533334.1:c.23C>T
NM_003331.4:c.1846C>T , LRG_121t1:c.1846C>T	NP_003322.3:p.Pro616Ser
XM_011528245.1:c.1846C>T	XP_011526547.1:p.Pro616Ser
XM_011528246.1:c.1549C>T	XP_011526548.1:p.Pro517Ser
XM_011528247.1:c.1549C>T	XP_011526549.1:p.Pro517Ser
XM_011528248.1:c.1846C>T	XP_011526550.1:p.Pro616Ser
XM_011528249.1:c.520C>T	XP_011526551.1:p.Pro174Ser
XM_011528250.1:c.1846C>T	XP_011526552.1:p.Pro616Ser
XM_011528251.1:c.150-47C>T	XP_011526553.1:n.150-47C>T
XM_011528252.1:c.1774-47C>T	XP_011526554.1:n.1774-47C>T
XM_011528246.3:c.1549C>T	XP_011526548.1:p.Pro517Ser
XM_011528249.2:c.520C>T	XP_011526551.1:p.Pro174Ser
XR_001753750.1:n.2003C>T
XR_001753751.1:n.2003C>T
XR_001753752.1:n.2003C>T
XR_002958353.1:n.1931-47C>T
NM_003331.5:c.1846C>T MANE Select	NP_003322.3:p.Pro616Ser
NM_001385197.1:c.1846C>T	NP_001372126.1:p.Pro616Ser
NM_001385198.1:c.1846C>T	NP_001372127.1:p.Pro616Ser
NM_001385199.1:c.1773+195C>T	NP_001372128.1:n.1773+195C>T
NM_001385200.1:c.1846C>T	NP_001372129.1:p.Pro616Ser
NM_001385201.1:c.1648C>T	NP_001372130.1:p.Pro550Ser
NM_001385202.1:c.1808+38C>T	NP_001372131.1:n.1808+38C>T
NM_001385203.1:c.1846C>T	NP_001372132.1:p.Pro616Ser
NM_001385204.1:c.1846C>T	NP_001372133.1:p.Pro616Ser
NM_001385205.1:c.1756C>T	NP_001372134.1:p.Pro586Ser
NM_001385206.1:c.1720C>T	NP_001372135.1:p.Pro574Ser
NM_001385207.1:c.1828C>T	NP_001372136.1:p.Pro610Ser