Linked Data
ClinVar Variation Id:
472906
dbSNP Id:
rs199636472
ExAC:
16:81925132 C / T
gnomAD v2:
16-81925132-C-T
gnomAD v3:
16-81891527-C-T
gnomAD v4:
16-81891527-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81891527C>T , CM000678.2:g.81891527C>T | GRCh38 |
| NC_000016.9:g.81925132C>T , CM000678.1:g.81925132C>T | GRCh37 |
| NC_000016.8:g.80482633C>T | NCBI36 |
| NG_032019.2:g.157431C>T , LRG_376:g.157431C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000563193.2:c.923C>T | ENSP00000455533.2:p.Ala308Val | |
| ENST00000697561.1:c.*352C>T | ENSP00000513337.1:n.*352C>T | |
| ENST00000697562.1:c.923C>T | ENSP00000513338.1:p.Ala308Val | |
| ENST00000697563.1:c.*769C>T | ENSP00000513339.1:n.*769C>T | |
| ENST00000697564.1:c.806C>T | ENSP00000513340.1:p.Ala269Val | |
| ENST00000697565.1:n.863C>T | ||
| ENST00000697581.1:c.*917C>T | ENSP00000513346.1:n.*917C>T | |
| ENST00000697582.1:c.923C>T | ENSP00000513347.1:p.Ala308Val | |
| ENST00000697583.1:c.722C>T | ENSP00000513349.1:p.Ala241Val | |
| ENST00000697584.1:c.722C>T | ENSP00000513350.1:p.Ala241Val | |
| ENST00000697585.1:c.722C>T | ENSP00000513351.1:p.Ala241Val | |
| ENST00000697586.1:c.722C>T | ENSP00000513352.1:p.Ala241Val | |
| ENST00000697587.1:c.722C>T | ENSP00000513353.1:p.Ala241Val | |
| ENST00000564138.6:c.923C>T MANE Select | ENSP00000482457.1:p.Ala308Val | |
| ENST00000359376.7:c.923C>T | ENSP00000352336.4:p.Ala308Val | |
| ENST00000562605.5:n.117C>T | ||
| ENST00000563193.1:c.231C>T | ||
| ENST00000564138.5:c.923C>T | ENSP00000482457.1:p.Ala308Val | |
| ENST00000567980.5:n.1167C>T | ||
| NM_002661.4:c.923C>T | NP_002652.2:p.Ala308Val | |
| XM_011523108.1:c.1037C>T | XP_011521410.1:p.Ala346Val | |
| NM_002661.5:c.923C>T MANE Select | NP_002652.2:p.Ala308Val |