Linked Data
ClinVar Variation Id:
315757
ClinVar RCV Id:
RCV000406820
dbSNP Id:
rs776375597
gnomAD v2:
15-38645762-C-T
gnomAD v3:
15-38353561-C-T
gnomAD v4:
15-38353561-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38353561C>T , CM000677.2:g.38353561C>T | GRCh38 |
| NC_000015.9:g.38645762C>T , CM000677.1:g.38645762C>T | GRCh37 |
| NC_000015.8:g.36433054C>T | NCBI36 |
| NG_008980.1:g.105711C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299084.9:c.*1897C>T MANE Select | ENSP00000299084.4:n.*1897C>T | |
| ENST00000299084.8:c.*1897C>T | ENSP00000299084.4:n.*1897C>T | |
| NM_152594.2:c.*1897C>T | NP_689807.1:n.*1897C>T | |
| XM_005254202.2:c.*1897C>T | XP_005254259.1:n.*1897C>T | |
| XM_005254203.3:c.*1897C>T | XP_005254260.1:n.*1897C>T | |
| XM_011521288.1:c.*1897C>T | XP_011519590.1:n.*1897C>T | |
| XM_011521289.1:c.*1897C>T | XP_011519591.1:n.*1897C>T | |
| XM_011521290.1:c.*1897C>T | XP_011519592.1:n.*1897C>T | |
| XM_005254202.3:c.*1897C>T | XP_005254259.1:n.*1897C>T | |
| XM_011521289.3:c.*1897C>T | XP_011519591.1:n.*1897C>T | |
| NM_152594.3:c.*1897C>T MANE Select | NP_689807.1:n.*1897C>T |