Linked Data
ClinVar Variation Id:
1626869
ClinVar RCV Id:
RCV002120638
dbSNP Id:
rs137853190
gnomAD v4:
6-63720626-A-G
MyVariant Identifiers:
chr6:g.64430522A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.63720626A>G , CM000668.2:g.63720626A>G | GRCh38 |
| NC_000006.11:g.64430522A>G , CM000668.1:g.64430522A>G | GRCh37 |
| NC_000006.10:g.64488481A>G | NCBI36 |
| NG_023443.1:g.1991597T>C | |
| NG_023443.2:g.1991600T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000262043.8:c.*6918A>G (PHF3) MANE Select | ENSP00000262043.4:n.*6918A>G | |
| ENST00000503581.6:c.9405T>C (EYS) MANE Select | ENSP00000424243.1:p.Tyr3135= | |
| ENST00000370616.6:c.9468T>C (EYS) | ENSP00000359650.2:p.Tyr3156= | |
| ENST00000370618.7:c.9405T>C (EYS) | ENSP00000359652.4:p.Tyr3135= | |
| ENST00000370621.7:c.9468T>C (EYS) | ENSP00000359655.3:p.Tyr3156= | |
| ENST00000503581.5:c.9405T>C (EYS) | ENSP00000424243.1:p.Tyr3135= | |
| ENST00000505138.1:c.363+9264A>G (PHF3) | ||
| NM_001142800.1:c.9405T>C (EYS) | NP_001136272.1:p.Tyr3135= | |
| NM_001292009.1:c.9468T>C (EYS) | NP_001278938.1:p.Tyr3156= | |
| NM_001142800.2:c.9405T>C (EYS) MANE Select | NP_001136272.1:p.Tyr3135= | |
| NM_001290259.2:c.*6918A>G (PHF3) | NP_001277188.1:n.*6918A>G | |
| NM_001370348.2:c.*6918A>G (PHF3) MANE Select | NP_001357277.1:n.*6918A>G | |
| NM_001370349.2:c.*6918A>G (PHF3) | NP_001357278.1:n.*6918A>G | |
| NM_001370350.2:c.*6918A>G (PHF3) | NP_001357279.1:n.*6918A>G | |
| NM_015153.4:c.*6918A>G (PHF3) | NP_055968.1:n.*6918A>G | |
| NM_001292009.2:c.9468T>C (EYS) | NP_001278938.1:p.Tyr3156= |