Linked Data
dbSNP Id:
rs2647257
gnomAD v2:
4-106199505-A-T
gnomAD v3:
4-105278348-A-T
gnomAD v4:
4-105278348-A-T
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 (TET2) MANE Select | ENSP00000369351.4:n.*1829A>T | |
| ENST00000265149.9:c.*4162A>T (TET2) | ENSP00000265149.5:n.*4162A>T | |
| ENST00000380013.8:c.*1829A>T (TET2) | ENSP00000369351.4:n.*1829A>T | |
| ENST00000513237.5:c.*1829A>T (TET2) | ENSP00000425443.1:n.*1829A>T | |
| ENST00000540549.5:c.*1829A>T (TET2) | ENSP00000442788.1:n.*1829A>T | |
| NM_001127208.2:c.*1829A>T , LRG_626t1:c.*1829A>T (TET2) | NP_001120680.1:n.*1829A>T | |
| NR_126420.1:n.318+56038T>A (TET2-AS1) | ||
| XM_005263082.1:c.*1829A>T (TET2) | XP_005263139.1:n.*1829A>T | |
| XM_006714242.2:c.*1829A>T (TET2) | XP_006714305.1:n.*1829A>T | |
| XM_011532044.1:c.*1829A>T (TET2) | XP_011530346.1:n.*1829A>T | |
| XR_244633.2:n.7740A>T (TET2) | ||
| XR_244634.2:n.8043A>T (TET2) | ||
| XM_005263082.3:c.*1829A>T (TET2) | XP_005263139.1:n.*1829A>T | |
| XM_006714242.3:c.*1829A>T (TET2) | XP_006714305.1:n.*1829A>T | |
| XM_024454102.1:c.*1829A>T (TET2) | XP_024309870.1:n.*1829A>T | |
| XM_024454103.1:c.*1829A>T (TET2) | XP_024309871.1:n.*1829A>T | |
| XR_244633.3:n.7775A>T (TET2) | ||
| NM_001127208.3:c.*1829A>T (TET2) MANE Select | NP_001120680.1:n.*1829A>T |