Linked Data
ClinVar Variation Id:
3074628
ClinVar RCV Id:
RCV004014162
dbSNP Id:
rs750809668
ExAC:
19:38946291 A / T
gnomAD v2:
19-38946291-A-T
gnomAD v4:
19-38455651-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38455651A>T , CM000681.2:g.38455651A>T | GRCh38 |
| NC_000019.9:g.38946291A>T , CM000681.1:g.38946291A>T | GRCh37 |
| NC_000019.8:g.43638131A>T | NCBI36 |
| NG_008866.1:g.26952A>T , LRG_766:g.26952A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.1691A>T | ENSP00000471601.2:p.Tyr564Phe | |
| ENST00000359596.8:c.1691A>T MANE Select | ENSP00000352608.2:p.Tyr564Phe | |
| ENST00000355481.8:c.1691A>T | ENSP00000347667.3:p.Tyr564Phe | |
| ENST00000359596.7:c.1691A>T | ENSP00000352608.2:p.Tyr564Phe | |
| ENST00000360985.7:c.1691A>T | ENSP00000354254.4:p.Tyr564Phe | |
| NM_000540.2:c.1691A>T , LRG_766t1:c.1691A>T | NP_000531.2:p.Tyr564Phe | |
| NM_001042723.1:c.1691A>T | NP_001036188.1:p.Tyr564Phe | |
| XM_006723317.1:c.1691A>T | XP_006723380.1:p.Tyr564Phe | |
| XM_006723319.1:c.1691A>T | XP_006723382.1:p.Tyr564Phe | |
| XM_011527204.1:c.1688A>T | XP_011525506.1:p.Tyr563Phe | |
| XM_011527205.1:c.1691A>T | XP_011525507.1:p.Tyr564Phe | |
| XM_006723317.2:c.1691A>T | XP_006723380.1:p.Tyr564Phe | |
| XM_006723319.2:c.1691A>T | XP_006723382.1:p.Tyr564Phe | |
| XM_011527205.2:c.1691A>T | XP_011525507.1:p.Tyr564Phe | |
| XR_001753735.1:n.1774A>T | ||
| NM_000540.3:c.1691A>T MANE Select | NP_000531.2:p.Tyr564Phe | |
| NM_001042723.2:c.1691A>T | NP_001036188.1:p.Tyr564Phe |