Linked Data
ClinVar Variation Id:
1523445
ClinVar RCV Id:
RCV002048916
dbSNP Id:
rs778172917
ExAC:
14:51095089 C / T
gnomAD v2:
14-51095089-C-T
gnomAD v4:
14-50628371-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50628371C>T , CM000676.2:g.50628371C>T | GRCh38 |
| NC_000014.8:g.51095089C>T , CM000676.1:g.51095089C>T | GRCh37 |
| NC_000014.7:g.50164839C>T | NCBI36 |
| NG_009028.1:g.100290C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553509.2:c.1460C>T | ENSP00000450989.2:p.Thr487Ile | |
| ENST00000556478.3:c.1460C>T | ENSP00000501428.2:p.Thr487Ile | |
| ENST00000682037.1:c.1460C>T | ENSP00000508289.1:p.Thr487Ile | |
| ENST00000682219.1:n.2798C>T | ||
| ENST00000683037.1:n.1381C>T | ||
| ENST00000683330.1:n.1794C>T | ||
| ENST00000358385.12:c.1460C>T MANE Select | ENSP00000351155.7:p.Thr487Ile | |
| ENST00000674288.1:c.*2752C>T | ENSP00000501522.1:n.*2752C>T | |
| ENST00000358385.10:c.1460C>T | ENSP00000351155.6:p.Thr487Ile | |
| ENST00000441560.6:c.1460C>T | ENSP00000413675.2:p.Thr487Ile | |
| ENST00000556067.1:c.206C>T | ENSP00000451100.1:p.Thr69Ile | |
| NM_001127713.1:c.1460C>T | NP_001121185.1:p.Thr487Ile | |
| NM_015915.4:c.1460C>T | NP_056999.2:p.Thr487Ile | |
| NM_181598.3:c.1460C>T | NP_853629.2:p.Thr487Ile | |
| NM_015915.5:c.1460C>T MANE Select | NP_056999.2:p.Thr487Ile | |
| NM_181598.4:c.1460C>T | NP_853629.2:p.Thr487Ile |