Canonical Allele Identifier: CA305194072

Gene: TYK2

Linked Data

• dbSNP Id: rs1048301147
• gnomAD v4: 19-10353816-G-C
• MyVariant Identifiers: chr19:g.10464492G>C (hg19) ; chr19:g.10353816G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10353816G>C , CM000681.2:g.10353816G>C	GRCh38
NC_000019.9:g.10464492G>C , CM000681.1:g.10464492G>C	GRCh37
NC_000019.8:g.10325492G>C	NCBI36
NG_007872.1:g.31757C>G , LRG_121:g.31757C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1258-170C>G	ENSP00000514307.1:n.*1258-170C>G
ENST00000525976.6:c.2909-170C>G	ENSP00000434831.2:n.2909-170C>G
ENST00000527481.3:c.2908+226C>G	ENSP00000466340.2:n.2908+226C>G
ENST00000529370.6:n.4285-170C>G
ENST00000529739.2:n.3548C>G
ENST00000530829.2:c.*2460-170C>G	ENSP00000436826.2:n.*2460-170C>G
ENST00000531836.6:c.2909-170C>G	ENSP00000436175.2:n.2909-170C>G
ENST00000533334.2:c.*951-170C>G	ENSP00000432320.2:n.*951-170C>G
ENST00000534228.2:n.4593C>G
ENST00000699354.1:n.1011-170C>G
ENST00000699355.1:c.*2239C>G	ENSP00000514328.1:n.*2239C>G
ENST00000699356.1:n.3548C>G
ENST00000699357.1:n.4593C>G
ENST00000699358.1:c.2909-170C>G	ENSP00000514329.1:n.2909-170C>G
ENST00000699359.1:c.115-170C>G
ENST00000699360.1:c.2909-170C>G	ENSP00000514331.1:n.2909-170C>G
ENST00000699364.1:n.25C>G
ENST00000699365.1:c.-26C>G	ENSP00000514334.1:n.-26C>G
ENST00000699366.1:n.109C>G
ENST00000699367.1:n.109C>G
ENST00000699368.1:c.226C>G	ENSP00000514335.1:n.226C>G
ENST00000525621.6:c.2909-170C>G MANE Select	ENSP00000431885.1:n.2909-170C>G
ENST00000264818.10:c.2909-170C>G	ENSP00000264818.6:n.2909-170C>G
ENST00000524462.5:c.2354-170C>G	ENSP00000433203.1:n.2354-170C>G
ENST00000525621.5:c.2909-170C>G	ENSP00000431885.1:n.2909-170C>G
ENST00000527481.2:c.204+226C>G
ENST00000529739.1:c.-193C>G	ENSP00000436155.1:n.-193C>G
ENST00000530560.5:c.337+226C>G	ENSP00000465291.1:n.337+226C>G
ENST00000592137.1:n.63-170C>G
NM_003331.4:c.2909-170C>G , LRG_121t1:c.2909-170C>G	NP_003322.3:n.2909-170C>G
XM_011528245.1:c.2909-170C>G	XP_011526547.1:n.2909-170C>G
XM_011528246.1:c.2612-170C>G	XP_011526548.1:n.2612-170C>G
XM_011528247.1:c.2612-170C>G	XP_011526549.1:n.2612-170C>G
XM_011528248.1:c.2909-170C>G	XP_011526550.1:n.2909-170C>G
XM_011528249.1:c.1583-170C>G	XP_011526551.1:n.1583-170C>G
XM_011528251.1:c.1166-170C>G	XP_011526553.1:n.1166-170C>G
XM_011528246.3:c.2612-170C>G	XP_011526548.1:n.2612-170C>G
XM_011528249.2:c.1583-170C>G	XP_011526551.1:n.1583-170C>G
XR_001753750.1:n.3066-170C>G
XR_001753751.1:n.3291C>G
XR_002958353.1:n.4217C>G
NM_003331.5:c.2909-170C>G MANE Select	NP_003322.3:n.2909-170C>G
NM_001385197.1:c.2909-170C>G	NP_001372126.1:n.2909-170C>G
NM_001385198.1:c.2909-170C>G	NP_001372127.1:n.2909-170C>G
NM_001385199.1:c.2723-170C>G	NP_001372128.1:n.2723-170C>G
NM_001385200.1:c.2906-170C>G	NP_001372129.1:n.2906-170C>G
NM_001385201.1:c.2711-170C>G	NP_001372130.1:n.2711-170C>G
NM_001385202.1:c.2825-170C>G	NP_001372131.1:n.2825-170C>G
NM_001385203.1:c.2990-170C>G	NP_001372132.1:n.2990-170C>G
NM_001385204.1:c.3119-170C>G	NP_001372133.1:n.3119-170C>G
NM_001385205.1:c.2819-170C>G	NP_001372134.1:n.2819-170C>G
NM_001385206.1:c.2783-170C>G	NP_001372135.1:n.2783-170C>G
NM_001385207.1:c.2891-170C>G	NP_001372136.1:n.2891-170C>G