Linked Data
ClinVar Variation Id:
502550
dbSNP Id:
rs185667326
ExAC:
14:21793998 G / A
gnomAD v2:
14-21793998-G-A
gnomAD v3:
14-21325839-G-A
gnomAD v4:
14-21325839-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.21325839G>A , CM000676.2:g.21325839G>A | GRCh38 |
| NC_000014.8:g.21793998G>A , CM000676.1:g.21793998G>A | GRCh37 |
| NC_000014.7:g.20863838G>A | NCBI36 |
| NG_008933.1:g.42863G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400017.7:c.2376G>A MANE Select | ENSP00000382895.2:p.Ser792= | |
| ENST00000382933.8:c.689-1784G>A | ENSP00000372391.4:n.689-1784G>A | |
| ENST00000400017.6:c.2376G>A | ENSP00000382895.2:p.Ser792= | |
| ENST00000553500.5:n.557G>A | ||
| ENST00000553927.1:n.1308G>A | ||
| ENST00000555322.5:c.803G>A | ||
| ENST00000555489.5:c.569G>A | ENSP00000451044.1:n.569G>A | |
| ENST00000555587.5:c.801G>A | ENSP00000451262.1:p.Ser267= | |
| ENST00000556336.5:c.1682-1784G>A | ENSP00000450445.1:n.1682-1784G>A | |
| ENST00000557771.5:c.2262G>A | ENSP00000451219.1:p.Ser754= | |
| NM_020366.3:c.2376G>A | NP_065099.3:p.Ser792= | |
| XM_005267879.2:c.1302G>A | XP_005267936.1:p.Ser434= | |
| XM_005267880.2:c.1269G>A | XP_005267937.1:p.Ser423= | |
| XM_005267881.2:c.750G>A | XP_005267938.1:p.Ser250= | |
| XM_011536978.1:c.1302G>A | XP_011535280.1:p.Ser434= | |
| XM_011536979.1:c.1086G>A | XP_011535281.1:p.Ser362= | |
| XM_011536980.1:c.957G>A | XP_011535282.1:p.Ser319= | |
| XM_011536981.1:c.1141+769G>A | XP_011535283.1:n.1141+769G>A | |
| XM_011536982.1:c.796+1114G>A | XP_011535284.1:n.796+1114G>A | |
| XM_011536983.1:c.2343G>A | XP_011535285.1:p.Ser781= | |
| XM_005267881.3:c.750G>A | XP_005267938.1:p.Ser250= | |
| XM_017021473.1:c.1141+769G>A | XP_016876962.1:n.1141+769G>A | |
| XM_024449663.1:c.1302G>A | XP_024305431.1:p.Ser434= | |
| XM_024449664.1:c.1141+769G>A | XP_024305432.1:n.1141+769G>A | |
| XM_024449665.1:c.796+1114G>A | XP_024305433.1:n.796+1114G>A | |
| XM_024449666.1:c.796+1114G>A | XP_024305434.1:n.796+1114G>A | |
| NM_001377523.1:c.689-1784G>A | NP_001364452.1:n.689-1784G>A | |
| NM_001377948.1:c.1302G>A | NP_001364877.1:p.Ser434= | |
| NM_001377949.1:c.796+1114G>A | NP_001364878.1:n.796+1114G>A | |
| NM_001377950.1:c.689-1784G>A | NP_001364879.1:n.689-1784G>A | |
| NM_001377951.1:c.191-1784G>A | NP_001364880.1:n.191-1784G>A | |
| NM_020366.4:c.2376G>A MANE Select | NP_065099.3:p.Ser792= |