Linked Data
ClinVar Variation Id:
329107
dbSNP Id:
rs757745087
ExAC:
19:39025806 C / T
gnomAD v2:
19-39025806-C-T
gnomAD v3:
19-38535166-C-T
gnomAD v4:
19-38535166-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38535166C>T , CM000681.2:g.38535166C>T | GRCh38 |
| NC_000019.9:g.39025806C>T , CM000681.1:g.39025806C>T | GRCh37 |
| NC_000019.8:g.43717646C>T | NCBI36 |
| NG_008866.1:g.106467C>T , LRG_766:g.106467C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.11324C>T | ENSP00000471601.2:n.11324C>T | |
| ENST00000359596.8:c.11385C>T MANE Select | ENSP00000352608.2:p.Ser3795= | |
| ENST00000355481.8:c.11370C>T | ENSP00000347667.3:p.Ser3790= | |
| ENST00000359596.7:c.11385C>T | ENSP00000352608.2:p.Ser3795= | |
| ENST00000360985.7:c.11367C>T | ENSP00000354254.4:p.Ser3789= | |
| ENST00000593322.1:c.86C>T | ||
| ENST00000594335.5:c.4772C>T | ||
| ENST00000596431.5:c.114C>T | ENSP00000470848.1:p.Ser38= | |
| ENST00000599547.5:c.2192C>T | ||
| ENST00000601514.5:c.666C>T | ENSP00000472497.1:p.Ser222= | |
| NM_000540.2:c.11385C>T , LRG_766t1:c.11385C>T | NP_000531.2:p.Ser3795= | |
| NM_001042723.1:c.11370C>T | NP_001036188.1:p.Ser3790= | |
| XM_006723317.1:c.11385C>T | XP_006723380.1:p.Ser3795= | |
| XM_006723319.1:c.11370C>T | XP_006723382.1:p.Ser3790= | |
| XM_011527204.1:c.11382C>T | XP_011525506.1:p.Ser3794= | |
| XM_011527205.1:c.11385C>T | XP_011525507.1:p.Ser3795= | |
| XM_006723317.2:c.11385C>T | XP_006723380.1:p.Ser3795= | |
| XM_006723319.2:c.11370C>T | XP_006723382.1:p.Ser3790= | |
| XM_011527205.2:c.11385C>T | XP_011525507.1:p.Ser3795= | |
| NM_000540.3:c.11385C>T MANE Select | NP_000531.2:p.Ser3795= | |
| NM_001042723.2:c.11370C>T | NP_001036188.1:p.Ser3790= |