Linked Data
ClinVar Variation Id:
197824
dbSNP Id:
rs151102991
ExAC:
16:49670687 G / A
gnomAD v2:
16-49670687-G-A
gnomAD v3:
16-49636776-G-A
gnomAD v4:
16-49636776-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.49636776G>A , CM000678.2:g.49636776G>A | GRCh38 |
| NC_000016.9:g.49670687G>A , CM000678.1:g.49670687G>A | GRCh37 |
| NC_000016.8:g.48228188G>A | NCBI36 |
| NG_032972.1:g.226144C>T | |
| NG_032972.2:g.226144C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000563137.7:c.2400C>T MANE Select | ENSP00000455588.3:p.Thr800= | |
| ENST00000262383.6:c.2376C>T | ENSP00000262383.2:p.Thr792= | |
| ENST00000535559.5:c.2025C>T | ENSP00000442321.1:p.Thr675= | |
| ENST00000561648.5:c.2376C>T | ENSP00000455426.1:p.Thr792= | |
| ENST00000562520.1:c.2196C>T | ENSP00000457664.1:p.Thr732= | |
| ENST00000562871.5:c.2196C>T | ENSP00000457928.1:p.Thr732= | |
| ENST00000563137.6:c.2196C>T | ENSP00000455588.2:p.Thr732= | |
| ENST00000567169.5:c.2025C>T | ENSP00000455061.1:p.Thr675= | |
| NM_001271620.1:c.2196C>T | NP_001258549.1:p.Thr732= | |
| NM_015069.3:c.2376C>T | NP_055884.2:p.Thr792= | |
| XM_005255856.3:c.2196C>T | XP_005255913.1:p.Thr732= | |
| XM_005255857.3:c.2025C>T | XP_005255914.1:p.Thr675= | |
| XM_006721171.2:c.2421C>T | XP_006721234.1:p.Thr807= | |
| XM_011522962.1:c.2469C>T | XP_011521264.1:p.Thr823= | |
| NM_001271620.2:c.2196C>T | NP_001258549.1:p.Thr732= | |
| NM_001330533.1:c.2025C>T | NP_001317462.1:p.Thr675= | |
| NM_015069.4:c.2376C>T | NP_055884.2:p.Thr792= | |
| XM_005255856.4:c.2196C>T | XP_005255913.1:p.Thr732= | |
| XM_006721171.4:c.2421C>T | XP_006721234.1:p.Thr807= | |
| XM_017023076.2:c.2400C>T | XP_016878565.1:p.Thr800= | |
| XM_017023077.1:c.2196C>T | XP_016878566.1:p.Thr732= | |
| XM_017023078.1:c.2196C>T | XP_016878567.1:p.Thr732= | |
| NM_001330533.2:c.2025C>T | NP_001317462.1:p.Thr675= | |
| NM_001379286.1:c.2400C>T MANE Select | NP_001366215.1:p.Thr800= | |
| NM_015069.5:c.2376C>T | NP_055884.2:p.Thr792= |