Linked Data
ClinVar Variation Id:
1623718
ClinVar RCV Id:
RCV002110271
dbSNP Id:
rs1768387033
gnomAD v3:
6-63721466-A-G
gnomAD v4:
6-63721466-A-G
MyVariant Identifiers:
chr6:g.64431362A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.63721466A>G , CM000668.2:g.63721466A>G | GRCh38 |
| NC_000006.11:g.64431362A>G , CM000668.1:g.64431362A>G | GRCh37 |
| NC_000006.10:g.64489321A>G | NCBI36 |
| NG_023443.1:g.1990757T>C | |
| NG_023443.2:g.1990760T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262043.8:c.*7758A>G (PHF3) MANE Select | ENSP00000262043.4:n.*7758A>G | |
| ENST00000503581.6:c.8565T>C (EYS) MANE Select | ENSP00000424243.1:p.Asn2855= | |
| ENST00000370616.6:c.8628T>C (EYS) | ENSP00000359650.2:p.Asn2876= | |
| ENST00000370618.7:c.8565T>C (EYS) | ENSP00000359652.4:p.Asn2855= | |
| ENST00000370621.7:c.8628T>C (EYS) | ENSP00000359655.3:p.Asn2876= | |
| ENST00000503581.5:c.8565T>C (EYS) | ENSP00000424243.1:p.Asn2855= | |
| ENST00000505138.1:c.363+10104A>G (PHF3) | ||
| NM_001142800.1:c.8565T>C (EYS) | NP_001136272.1:p.Asn2855= | |
| NM_001292009.1:c.8628T>C (EYS) | NP_001278938.1:p.Asn2876= | |
| NM_001142800.2:c.8565T>C (EYS) MANE Select | NP_001136272.1:p.Asn2855= | |
| NM_001290259.2:c.*7758A>G (PHF3) | NP_001277188.1:n.*7758A>G | |
| NM_001370348.2:c.*7758A>G (PHF3) MANE Select | NP_001357277.1:n.*7758A>G | |
| NM_001370349.2:c.*7758A>G (PHF3) | NP_001357278.1:n.*7758A>G | |
| NM_001370350.2:c.*7758A>G (PHF3) | NP_001357279.1:n.*7758A>G | |
| NM_015153.4:c.*7758A>G (PHF3) | NP_055968.1:n.*7758A>G | |
| NM_001292009.2:c.8628T>C (EYS) | NP_001278938.1:p.Asn2876= |