Linked Data
ClinVar Variation Id:
1078220
ClinVar RCV Id:
RCV001393042
dbSNP Id:
rs752761440
ExAC:
14:51095081 C / T
gnomAD v2:
14-51095081-C-T
gnomAD v3:
14-50628363-C-T
gnomAD v4:
14-50628363-C-T
COSMIC:
COSM4577874
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50628363C>T , CM000676.2:g.50628363C>T | GRCh38 |
| NC_000014.8:g.51095081C>T , CM000676.1:g.51095081C>T | GRCh37 |
| NC_000014.7:g.50164831C>T | NCBI36 |
| NG_009028.1:g.100282C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553509.2:c.1452C>T | ENSP00000450989.2:p.Thr484= | |
| ENST00000556478.3:c.1452C>T | ENSP00000501428.2:p.Thr484= | |
| ENST00000682037.1:c.1452C>T | ENSP00000508289.1:p.Thr484= | |
| ENST00000682219.1:n.2790C>T | ||
| ENST00000683037.1:n.1373C>T | ||
| ENST00000683330.1:n.1786C>T | ||
| ENST00000358385.12:c.1452C>T MANE Select | ENSP00000351155.7:p.Thr484= | |
| ENST00000674288.1:c.*2744C>T | ENSP00000501522.1:n.*2744C>T | |
| ENST00000358385.10:c.1452C>T | ENSP00000351155.6:p.Thr484= | |
| ENST00000441560.6:c.1452C>T | ENSP00000413675.2:p.Thr484= | |
| ENST00000556067.1:c.198C>T | ENSP00000451100.1:p.Thr66= | |
| NM_001127713.1:c.1452C>T | NP_001121185.1:p.Thr484= | |
| NM_015915.4:c.1452C>T | NP_056999.2:p.Thr484= | |
| NM_181598.3:c.1452C>T | NP_853629.2:p.Thr484= | |
| NM_015915.5:c.1452C>T MANE Select | NP_056999.2:p.Thr484= | |
| NM_181598.4:c.1452C>T | NP_853629.2:p.Thr484= |