Canonical Allele Identifier: CA103367783
Gene: TET2 HGNC NCBI

Linked Data

dbSNP Id: rs9790517

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105163621C>T , CM000666.2:g.105163621C>T GRCh38
NC_000004.11:g.106084778C>T , CM000666.1:g.106084778C>T GRCh37
NC_000004.10:g.106304227C>T NCBI36
NG_028191.1:g.22747C>T , LRG_626:g.22747C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265149.9:c.-193+16642C>T ENSP00000265149.5:p.=
ENST00000305737.6:c.-193+17535C>T ENSP00000306705.2:p.=
ENST00000380013.8:c.-193+16642C>T ENSP00000369351.4:p.=
ENST00000394764.2:c.-47+16642C>T ENSP00000378245.2:p.=
ENST00000413648.2:c.-47+16642C>T ENSP00000391448.2:p.=
ENST00000513237.5:c.-111+16642C>T ENSP00000425443.1:p.=
ENST00000514870.1:c.-193+15822C>T ENSP00000426885.1:p.=
ENST00000540549.5:c.-174+16642C>T ENSP00000442788.1:p.=
NM_001127208.2:c.-193+16642C>T , LRG_626t1:c.-193+16642C>T NP_001120680.1:p.=
NM_017628.4:c.-193+17535C>T , LRG_626t2:c.-193+17535C>T NP_060098.3:p.=
XM_005263082.1:c.-47+16642C>T XP_005263139.1:p.=
XM_006714242.2:c.-193+16642C>T XP_006714305.1:p.=
XM_011532043.1:c.-193+16642C>T XP_011530345.1:p.=
XM_005263082.3:c.-47+16642C>T XP_005263139.1:p.=
XM_006714242.3:c.-193+16642C>T XP_006714305.1:p.=
XM_017008319.1:c.-193+16642C>T XP_016863808.1:p.=
XM_024454102.1:c.-305-8194C>T XP_024309870.1:p.=
XM_024454103.1:c.-193+17535C>T XP_024309871.1:p.=
NM_001127208.3:c.-193+16642C>T MANE Select NP_001120680.1:p.=