Linked Data
dbSNP Id:
rs1201805392
gnomAD v2:
17-6328885-T-A
gnomAD v3:
17-6425565-T-A
gnomAD v4:
17-6425565-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6425565T>A , CM000679.2:g.6425565T>A | GRCh38 |
| NC_000017.10:g.6328885T>A , CM000679.1:g.6328885T>A | GRCh37 |
| NC_000017.9:g.6269609T>A | NCBI36 |
| NG_008474.1:g.14635A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000381129.8:c.1050A>T MANE Select | ENSP00000370521.3:p.Pro350= | |
| ENST00000250087.9:c.861A>T | ENSP00000250087.5:p.Pro287= | |
| ENST00000381128.2:c.*922A>T | ENSP00000370520.2:n.*922A>T | |
| ENST00000381129.7:c.1050A>T | ENSP00000370521.3:p.Pro350= | |
| ENST00000570466.5:c.984A>T | ENSP00000461287.1:p.Pro328= | |
| ENST00000570584.5:c.251+8354A>T | ||
| ENST00000574506.5:c.1014A>T | ENSP00000458456.1:p.Pro338= | |
| ENST00000575265.5:c.*1021A>T | ENSP00000459673.1:n.*1021A>T | |
| ENST00000576307.5:c.870A>T | ENSP00000459522.1:p.Pro290= | |
| ENST00000576776.5:c.978A>T | ENSP00000460827.1:p.Pro326= | |
| ENST00000621374.4:c.*68A>T | ENSP00000481337.1:n.*68A>T | |
| NM_001033054.2:c.861A>T | NP_001028226.1:p.Pro287= | |
| NM_001033055.2:c.870A>T | NP_001028227.1:p.Pro290= | |
| NM_001285399.2:c.1014A>T | NP_001272328.1:p.Pro338= | |
| NM_001285400.2:c.984A>T | NP_001272329.1:p.Pro328= | |
| NM_001285401.2:c.978A>T | NP_001272330.1:p.Pro326= | |
| NM_001285402.1:c.933A>T | NP_001272331.1:p.Pro311= | |
| NM_014336.4:c.1050A>T | NP_055151.3:p.Pro350= | |
| NM_001033054.3:c.861A>T | NP_001028226.1:p.Pro287= | |
| NM_001033055.3:c.870A>T | NP_001028227.1:p.Pro290= | |
| NM_001285399.3:c.1014A>T | NP_001272328.1:p.Pro338= | |
| NM_001285400.3:c.984A>T | NP_001272329.1:p.Pro328= | |
| NM_001285401.3:c.978A>T | NP_001272330.1:p.Pro326= | |
| NM_001285402.2:c.933A>T | NP_001272331.1:p.Pro311= | |
| NM_001285403.3:c.*1021A>T | NP_001272332.1:n.*1021A>T | |
| NM_014336.5:c.1050A>T MANE Select | NP_055151.3:p.Pro350= | |
| NM_001285403.4:c.*1021A>T | NP_001272332.1:n.*1021A>T |