Canonical Allele Identifier: CA102740632
Gene: TET2 HGNC NCBI
TET2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2647257

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105278348A>T , CM000666.2:g.105278348A>T GRCh38
NC_000004.11:g.106199505A>T , CM000666.1:g.106199505A>T GRCh37
NC_000004.10:g.106418954A>T NCBI36
NG_028191.1:g.137474A>T , LRG_626:g.137474A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380013.9:c.*1829A>T MANE Select ENSP00000369351.4:p.=
ENST00000265149.9:c.*4162A>T ENSP00000265149.5:p.=
ENST00000380013.8:c.*1829A>T ENSP00000369351.4:p.=
ENST00000513237.5:c.*1829A>T ENSP00000425443.1:p.=
ENST00000540549.5:c.*1829A>T ENSP00000442788.1:p.=
NM_001127208.2:c.*1829A>T , LRG_626t1:c.*1829A>T (TET2) NP_001120680.1:p.=
NR_126420.1:n.318+56038T>A (TET2-AS1)
XM_005263082.1:c.*1829A>T (TET2) XP_005263139.1:p.=
XM_006714242.2:c.*1829A>T (TET2) XP_006714305.1:p.=
XM_011532044.1:c.*1829A>T (TET2) XP_011530346.1:p.=
XR_244633.2:n.7740A>T (TET2)
XR_244634.2:n.8043A>T (TET2)
XM_005263082.3:c.*1829A>T (TET2) XP_005263139.1:p.=
XM_006714242.3:c.*1829A>T (TET2) XP_006714305.1:p.=
XM_024454102.1:c.*1829A>T (TET2) XP_024309870.1:p.=
XM_024454103.1:c.*1829A>T (TET2) XP_024309871.1:p.=
XR_244633.3:n.7775A>T (TET2)
NM_001127208.3:c.*1829A>T (TET2) MANE Select NP_001120680.1:p.=