Linked Data
ClinVar Variation Id:
464038
dbSNP Id:
rs142712849
ExAC:
10:97380991 G / C
gnomAD v2:
10-97380991-G-C
gnomAD v3:
10-95621234-G-C
gnomAD v4:
10-95621234-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.95621234G>C , CM000672.2:g.95621234G>C | GRCh38 |
| NC_000010.10:g.97380991G>C , CM000672.1:g.97380991G>C | GRCh37 |
| NC_000010.9:g.97370981G>C | NCBI36 |
| NG_012258.1:g.40577C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371224.7:c.1264C>G MANE Select | ENSP00000360268.2:p.Leu422Val | |
| ENST00000371221.3:c.1258C>G | ENSP00000360265.3:p.Leu420Val | |
| ENST00000371224.6:c.1264C>G | ENSP00000360268.2:p.Leu422Val | |
| NM_001017423.1:c.1258C>G | NP_001017423.1:p.Leu420Val | |
| NM_002860.3:c.1264C>G | NP_002851.2:p.Leu422Val | |
| XM_006717933.1:c.1264C>G | XP_006717996.1:p.Leu422Val | |
| XM_011540001.1:c.931C>G | XP_011538303.1:p.Leu311Val | |
| NM_001323412.1:c.931C>G | NP_001310341.1:p.Leu311Val | |
| NM_001323413.1:c.1264C>G | NP_001310342.1:p.Leu422Val | |
| NM_001323414.1:c.1264C>G | NP_001310343.1:p.Leu422Val | |
| NM_001323415.1:c.1258C>G | NP_001310344.1:p.Leu420Val | |
| NM_001323416.1:c.931C>G | NP_001310345.1:p.Leu311Val | |
| NM_001323417.1:c.1159C>G | NP_001310346.1:p.Leu387Val | |
| NM_001323418.1:c.925C>G | NP_001310347.1:p.Leu309Val | |
| NM_001323419.1:c.628C>G | NP_001310348.1:p.Leu210Val | |
| XM_024448094.1:c.1264C>G | XP_024303862.1:p.Leu422Val | |
| XM_024448095.1:c.1264C>G | XP_024303863.1:p.Leu422Val | |
| XM_024448096.1:c.1258C>G | XP_024303864.1:p.Leu420Val | |
| XM_024448097.1:c.931C>G | XP_024303865.1:p.Leu311Val | |
| NM_002860.4:c.1264C>G MANE Select | NP_002851.2:p.Leu422Val | |
| NM_001017423.2:c.1258C>G | NP_001017423.1:p.Leu420Val | |
| NM_001323412.2:c.931C>G | NP_001310341.1:p.Leu311Val | |
| NM_001323413.2:c.1264C>G | NP_001310342.1:p.Leu422Val | |
| NM_001323414.2:c.1264C>G | NP_001310343.1:p.Leu422Val | |
| NM_001323415.2:c.1258C>G | NP_001310344.1:p.Leu420Val | |
| NM_001323416.2:c.931C>G | NP_001310345.1:p.Leu311Val | |
| NM_001323417.2:c.1159C>G | NP_001310346.1:p.Leu387Val | |
| NM_001323418.2:c.925C>G | NP_001310347.1:p.Leu309Val | |
| NM_001323419.2:c.628C>G | NP_001310348.1:p.Leu210Val |