Canonical Allele Identifier: CA2602879820
Gene: TET2 HGNC NCBI

Linked Data

dbSNP Id: rs760549979

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105163696C>A , CM000666.2:g.105163696C>A GRCh38
NC_000004.11:g.106084853C>A , CM000666.1:g.106084853C>A GRCh37
NC_000004.10:g.106304302C>A NCBI36
NG_028191.1:g.22822C>A , LRG_626:g.22822C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380013.9:c.-193+16717C>A MANE Select ENSP00000369351.4:n.-193+16717C>A
ENST00000265149.9:c.-193+16717C>A ENSP00000265149.5:n.-193+16717C>A
ENST00000305737.6:c.-193+17610C>A ENSP00000306705.2:n.-193+17610C>A
ENST00000380013.8:c.-193+16717C>A ENSP00000369351.4:n.-193+16717C>A
ENST00000394764.2:c.-47+16717C>A ENSP00000378245.2:n.-47+16717C>A
ENST00000413648.2:c.-47+16717C>A ENSP00000391448.2:n.-47+16717C>A
ENST00000504042.5:n.102+16717C>A
ENST00000505801.1:n.47+16717C>A
ENST00000513237.5:c.-111+16717C>A ENSP00000425443.1:n.-111+16717C>A
ENST00000514870.1:c.-193+15897C>A ENSP00000426885.1:n.-193+15897C>A
ENST00000540549.5:c.-174+16717C>A ENSP00000442788.1:n.-174+16717C>A
NM_001127208.2:c.-193+16717C>A , LRG_626t1:c.-193+16717C>A NP_001120680.1:n.-193+16717C>A
NM_017628.4:c.-193+17610C>A , LRG_626t2:c.-193+17610C>A NP_060098.3:n.-193+17610C>A
XM_005263082.1:c.-47+16717C>A XP_005263139.1:n.-47+16717C>A
XM_006714242.2:c.-193+16717C>A XP_006714305.1:n.-193+16717C>A
XM_011532043.1:c.-193+16717C>A XP_011530345.1:n.-193+16717C>A
XR_244633.2:n.104+16717C>A
XR_244634.2:n.104+16717C>A
XR_427546.2:n.104+16717C>A
XR_938746.1:n.104+16717C>A
XR_938747.1:n.104+16717C>A
XM_005263082.3:c.-47+16717C>A XP_005263139.1:n.-47+16717C>A
XM_006714242.3:c.-193+16717C>A XP_006714305.1:n.-193+16717C>A
XM_017008319.1:c.-193+16717C>A XP_016863808.1:n.-193+16717C>A
XM_024454102.1:c.-305-8119C>A XP_024309870.1:n.-305-8119C>A
XM_024454103.1:c.-193+17610C>A XP_024309871.1:n.-193+17610C>A
XR_001741246.1:n.139+16717C>A
XR_244633.3:n.139+16717C>A
XR_427546.4:n.139+16717C>A
XR_938746.2:n.139+16717C>A
XR_938747.3:n.139+16717C>A
NM_001127208.3:c.-193+16717C>A MANE Select NP_001120680.1:n.-193+16717C>A