Linked Data
ClinVar Variation Id:
1714509
ClinVar RCV Id:
RCV002295625
dbSNP Id:
rs1233556369
gnomAD v2:
17-40695964-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42543946C>T , CM000679.2:g.42543946C>T | GRCh38 |
| NC_000017.10:g.40695964C>T , CM000679.1:g.40695964C>T | GRCh37 |
| NC_000017.9:g.37949490C>T | NCBI36 |
| NG_011552.1:g.13014C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.1940C>T MANE Select | ENSP00000225927.1:p.Thr647Ile | |
| ENST00000225927.6:c.1940C>T | ENSP00000225927.1:p.Thr647Ile | |
| ENST00000591587.1:c.1278C>T | ENSP00000467836.1:n.1278C>T | |
| NM_000263.3:c.1940C>T | NP_000254.2:p.Thr647Ile | |
| XM_006721920.2:c.1109C>T | XP_006721983.1:p.Thr370Ile | |
| XM_011524840.1:c.941C>T | XP_011523142.1:p.Thr314Ile | |
| XM_017024687.1:c.1109C>T | XP_016880176.1:p.Thr370Ile | |
| XM_024450771.1:c.1997C>T | XP_024306539.1:p.Thr666Ile | |
| XM_024450772.1:c.941C>T | XP_024306540.1:p.Thr314Ile | |
| NM_000263.4:c.1940C>T MANE Select | NP_000254.2:p.Thr647Ile |