Linked Data
ClinVar Variation Id:
1605872
ClinVar RCV Id:
RCV002151998
dbSNP Id:
rs2143077498
gnomAD v4:
17-42536611-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536611A>T , CM000679.2:g.42536611A>T | GRCh38 |
| NC_000017.10:g.40688629A>T , CM000679.1:g.40688629A>T | GRCh37 |
| NC_000017.9:g.37942155A>T | NCBI36 |
| NG_011552.1:g.5679A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.339A>T MANE Select | ENSP00000225927.1:p.Pro113= | |
| ENST00000225927.6:c.339A>T | ENSP00000225927.1:p.Pro113= | |
| ENST00000586516.5:c.89A>T | ||
| ENST00000591587.1:c.82A>T | ENSP00000467836.1:p.Thr28Ser | |
| NM_000263.3:c.339A>T | NP_000254.2:p.Pro113= | |
| XM_006721920.2:c.-404A>T | XP_006721983.1:n.-404A>T | |
| XM_011524840.1:c.-404A>T | XP_011523142.1:n.-404A>T | |
| XM_024450771.1:c.339A>T | XP_024306539.1:p.Pro113= | |
| NM_000263.4:c.339A>T MANE Select | NP_000254.2:p.Pro113= |