Linked Data
ClinVar Variation Id:
324587
dbSNP Id:
rs4577135
gnomAD v2:
17-6327771-T-C
gnomAD v3:
17-6424451-T-C
gnomAD v4:
17-6424451-T-C
Allelic Epigenome:
Alellic Epigenome (raw data)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6424451T>C , CM000679.2:g.6424451T>C | GRCh38 |
| NC_000017.10:g.6327771T>C , CM000679.1:g.6327771T>C | GRCh37 |
| NC_000017.9:g.6268495T>C | NCBI36 |
| NG_008474.1:g.15749A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381129.8:c.*1009A>G MANE Select | ENSP00000370521.3:n.*1009A>G | |
| ENST00000250087.9:c.*1009A>G | ENSP00000250087.5:n.*1009A>G | |
| ENST00000381128.2:c.*2036A>G | ENSP00000370520.2:n.*2036A>G | |
| ENST00000381129.7:c.*1009A>G | ENSP00000370521.3:n.*1009A>G | |
| ENST00000570584.5:c.251+9468A>G | ||
| NM_001033054.2:c.*1009A>G | NP_001028226.1:n.*1009A>G | |
| NM_001033055.2:c.*1009A>G | NP_001028227.1:n.*1009A>G | |
| NM_001285399.2:c.*1009A>G | NP_001272328.1:n.*1009A>G | |
| NM_001285400.2:c.*1009A>G | NP_001272329.1:n.*1009A>G | |
| NM_001285401.2:c.*1009A>G | NP_001272330.1:n.*1009A>G | |
| NM_001285402.1:c.*1009A>G | NP_001272331.1:n.*1009A>G | |
| NM_014336.4:c.*1009A>G | NP_055151.3:n.*1009A>G | |
| NM_001033054.3:c.*1009A>G | NP_001028226.1:n.*1009A>G | |
| NM_001033055.3:c.*1009A>G | NP_001028227.1:n.*1009A>G | |
| NM_001285399.3:c.*1009A>G | NP_001272328.1:n.*1009A>G | |
| NM_001285400.3:c.*1009A>G | NP_001272329.1:n.*1009A>G | |
| NM_001285401.3:c.*1009A>G | NP_001272330.1:n.*1009A>G | |
| NM_001285402.2:c.*1009A>G | NP_001272331.1:n.*1009A>G | |
| NM_014336.5:c.*1009A>G MANE Select | NP_055151.3:n.*1009A>G |