Linked Data
dbSNP Id:
rs200382777
gnomAD v2:
15-78894332-C-A
gnomAD v3:
15-78601990-C-A
gnomAD v4:
15-78601990-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.78601990C>A , CM000677.2:g.78601990C>A | GRCh38 |
| NC_000015.9:g.78894332C>A , CM000677.1:g.78894332C>A | GRCh37 |
| NC_000015.8:g.76681387C>A | NCBI36 |
| NG_016143.1:g.24306G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326828.6:c.652G>T MANE Select | ENSP00000315602.5:p.Asp218Tyr | |
| ENST00000326828.5:c.652G>T | ENSP00000315602.5:p.Asp218Tyr | |
| ENST00000348639.7:c.652G>T | ENSP00000267951.4:p.Asp218Tyr | |
| ENST00000558903.1:n.359G>T | ||
| ENST00000559658.5:c.652G>T | ENSP00000452896.1:p.Asp218Tyr | |
| NM_000743.4:c.652G>T | NP_000734.2:p.Asp218Tyr | |
| NM_001166694.1:c.652G>T | NP_001160166.1:p.Asp218Tyr | |
| NR_046313.1:n.1153G>T | ||
| XM_006720382.1:c.451G>T | XP_006720445.1:p.Asp151Tyr | |
| XM_011521173.1:c.571G>T | XP_011519475.1:p.Asp191Tyr | |
| XM_006720382.3:c.451G>T | XP_006720445.1:p.Asp151Tyr | |
| NM_000743.5:c.652G>T MANE Select | NP_000734.2:p.Asp218Tyr | |
| NM_001166694.2:c.652G>T | NP_001160166.1:p.Asp218Tyr | |
| NR_046313.2:n.854G>T |