Linked Data
ClinVar Variation Id:
1022145
ClinVar RCV Id:
RCV001322016
dbSNP Id:
rs1911829075
MyVariant Identifiers:
chr17:g.6328840C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6425520C>A , CM000679.2:g.6425520C>A | GRCh38 |
| NC_000017.10:g.6328840C>A , CM000679.1:g.6328840C>A | GRCh37 |
| NC_000017.9:g.6269564C>A | NCBI36 |
| NG_008474.1:g.14680G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381129.8:c.1095G>T MANE Select | ENSP00000370521.3:p.Gly365= | |
| ENST00000250087.9:c.906G>T | ENSP00000250087.5:p.Gly302= | |
| ENST00000381128.2:c.*967G>T | ENSP00000370520.2:n.*967G>T | |
| ENST00000381129.7:c.1095G>T | ENSP00000370521.3:p.Gly365= | |
| ENST00000570466.5:c.1029G>T | ENSP00000461287.1:p.Gly343= | |
| ENST00000570584.5:c.251+8399G>T | ||
| ENST00000574506.5:c.1059G>T | ENSP00000458456.1:p.Gly353= | |
| ENST00000575265.5:c.*1066G>T | ENSP00000459673.1:n.*1066G>T | |
| ENST00000576307.5:c.915G>T | ENSP00000459522.1:p.Gly305= | |
| ENST00000576776.5:c.1023G>T | ENSP00000460827.1:p.Gly341= | |
| ENST00000621374.4:c.*113G>T | ENSP00000481337.1:n.*113G>T | |
| NM_001033054.2:c.906G>T | NP_001028226.1:p.Gly302= | |
| NM_001033055.2:c.915G>T | NP_001028227.1:p.Gly305= | |
| NM_001285399.2:c.1059G>T | NP_001272328.1:p.Gly353= | |
| NM_001285400.2:c.1029G>T | NP_001272329.1:p.Gly343= | |
| NM_001285401.2:c.1023G>T | NP_001272330.1:p.Gly341= | |
| NM_001285402.1:c.978G>T | NP_001272331.1:p.Gly326= | |
| NM_014336.4:c.1095G>T | NP_055151.3:p.Gly365= | |
| NM_001033054.3:c.906G>T | NP_001028226.1:p.Gly302= | |
| NM_001033055.3:c.915G>T | NP_001028227.1:p.Gly305= | |
| NM_001285399.3:c.1059G>T | NP_001272328.1:p.Gly353= | |
| NM_001285400.3:c.1029G>T | NP_001272329.1:p.Gly343= | |
| NM_001285401.3:c.1023G>T | NP_001272330.1:p.Gly341= | |
| NM_001285402.2:c.978G>T | NP_001272331.1:p.Gly326= | |
| NM_001285403.3:c.*1066G>T | NP_001272332.1:n.*1066G>T | |
| NM_014336.5:c.1095G>T MANE Select | NP_055151.3:p.Gly365= | |
| NM_001285403.4:c.*1066G>T | NP_001272332.1:n.*1066G>T |