Linked Data
ClinVar Variation Id:
1210206
ClinVar RCV Id:
RCV001580258
dbSNP Id:
rs770992614
ExAC:
17:45363673 C / T
gnomAD v2:
17-45363673-C-T
gnomAD v3:
17-47286307-C-T
gnomAD v4:
17-47286307-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47286307C>T , CM000679.2:g.47286307C>T | GRCh38 |
| NC_000017.10:g.45363673C>T , CM000679.1:g.45363673C>T | GRCh37 |
| NC_000017.9:g.42718672C>T | NCBI36 |
| NG_008332.2:g.37466C>T , LRG_481:g.37466C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.662C>T | ENSP00000513002.1:p.Thr221Met | |
| ENST00000559488.7:c.662C>T MANE Select | ENSP00000452786.2:p.Thr221Met | |
| ENST00000559488.5:c.662C>T | ENSP00000452786.1:p.Thr221Met | |
| ENST00000560629.1:c.627C>T | ||
| ENST00000571680.1:c.662C>T | ENSP00000461626.1:p.Thr221Met | |
| NM_000212.2:c.662C>T , LRG_481t1:c.662C>T | NP_000203.2:p.Thr221Met | |
| NM_000212.3:c.662C>T MANE Select | NP_000203.2:p.Thr221Met |