Linked Data
ClinVar Variation Id:
415414
dbSNP Id:
rs375091696
ExAC:
9:139399487 C / T
gnomAD v2:
9-139399487-C-T
gnomAD v3:
9-136505035-C-T
gnomAD v4:
9-136505035-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136505035C>T , CM000671.2:g.136505035C>T | GRCh38 |
| NC_000009.11:g.139399487C>T , CM000671.1:g.139399487C>T | GRCh37 |
| NC_000009.10:g.138519308C>T | NCBI36 |
| NG_007458.1:g.45752G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645828.1:n.2463G>A | ||
| ENST00000651671.1:c.4656G>A MANE Select | ENSP00000498587.1:p.Ala1552= | |
| ENST00000679595.1:c.4656G>A | ENSP00000506241.1:p.Ala1552= | |
| ENST00000680133.1:c.4542G>A | ENSP00000505319.1:p.Ala1514= | |
| ENST00000680218.1:c.4536G>A | ENSP00000505339.1:p.Ala1512= | |
| ENST00000680668.1:c.4542G>A | ENSP00000506336.1:p.Ala1514= | |
| ENST00000680778.1:c.2253G>A | ENSP00000506033.1:p.Ala751= | |
| ENST00000680924.1:c.*2056G>A | ENSP00000506031.1:n.*2056G>A | |
| ENST00000681135.1:c.*2265G>A | ENSP00000506636.1:n.*2265G>A | |
| ENST00000681298.1:n.1469G>A | ||
| ENST00000681454.1:c.*3892G>A | ENSP00000505763.1:n.*3892G>A | |
| ENST00000277541.6:c.4656G>A | ENSP00000277541.6:p.Ala1552= | |
| NM_017617.3:c.4656G>A | NP_060087.3:p.Ala1552= | |
| XM_011518717.1:c.3957G>A | XP_011517019.1:p.Ala1319= | |
| NM_017617.5:c.4656G>A MANE Select | NP_060087.3:p.Ala1552= | |
| XM_011518717.2:c.3933G>A | XP_011517019.2:p.Ala1311= |