Linked Data
ClinVar Variation Id:
471872
dbSNP Id:
rs374309472
ExAC:
5:1266581 G / A
gnomAD v2:
5-1266581-G-A
gnomAD v3:
5-1266466-G-A
gnomAD v4:
5-1266466-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1266466G>A , CM000667.2:g.1266466G>A | GRCh38 |
| NC_000005.9:g.1266581G>A , CM000667.1:g.1266581G>A | GRCh37 |
| NC_000005.8:g.1319581G>A | NCBI36 |
| NG_009265.1:g.33582C>T , LRG_343:g.33582C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310581.10:c.2652C>T MANE Select | ENSP00000309572.5:p.Leu884= | |
| ENST00000656021.1:c.*2198C>T | ENSP00000499759.1:n.*2198C>T | |
| ENST00000310581.9:c.2652C>T | ENSP00000309572.5:p.Leu884= | |
| ENST00000334602.10:c.2652C>T | ENSP00000334346.6:p.Leu884= | |
| ENST00000460137.6:c.2434C>T | ENSP00000425003.1:n.2434C>T | |
| ENST00000484238.6:n.1283C>T | ||
| ENST00000503656.1:n.59C>T | ||
| ENST00000508104.2:c.2470C>T | ENSP00000426042.2:n.2470C>T | |
| NM_001193376.1:c.2652C>T | NP_001180305.1:p.Leu884= | |
| NM_198253.2:c.2652C>T , LRG_343t1:c.2652C>T | NP_937983.2:p.Leu884= | |
| XM_011514104.1:c.1122C>T | XP_011512406.1:p.Leu374= | |
| XM_011514105.1:c.1008C>T | XP_011512407.1:p.Leu336= | |
| XM_011514106.1:c.1008C>T | XP_011512408.1:p.Leu336= | |
| NR_149162.1:n.2528C>T | ||
| NR_149163.1:n.2492C>T | ||
| NM_001193376.2:c.2652C>T | NP_001180305.1:p.Leu884= | |
| NM_198253.3:c.2652C>T MANE Select | NP_937983.2:p.Leu884= | |
| NR_149162.2:n.2549C>T | ||
| NR_149163.2:n.2513C>T | ||
| NM_001193376.3:c.2652C>T | NP_001180305.1:p.Leu884= | |
| NR_149162.3:n.2549C>T | ||
| NR_149163.3:n.2513C>T |