Linked Data
ClinVar Variation Id:
2856972
ClinVar RCV Id:
RCV003743139
dbSNP Id:
rs1765327994
gnomAD v3:
5-112838655-C-G
gnomAD v4:
5-112838655-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838655C>G , CM000667.2:g.112838655C>G | GRCh38 |
| NC_000005.9:g.112174352C>G , CM000667.1:g.112174352C>G | GRCh37 |
| NC_000005.8:g.112202251C>G | NCBI36 |
| NG_008481.4:g.151135C>G , LRG_130:g.151135C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.2726C>G | ENSP00000484935.2:n.2726C>G | |
| ENST00000504915.3:c.3115C>G | ENSP00000473355.2:p.Leu1039Val | |
| ENST00000505350.2:c.*3067C>G | ENSP00000481752.1:n.*3067C>G | |
| ENST00000507379.6:c.3007C>G | ENSP00000423224.2:p.Leu1003Val | |
| ENST00000509732.6:c.3061C>G | ENSP00000426541.2:p.Leu1021Val | |
| ENST00000512211.7:c.3061C>G | ENSP00000423828.3:p.Leu1021Val | |
| ENST00000257430.9:c.3061C>G MANE Select | ENSP00000257430.4:p.Leu1021Val | |
| ENST00000257430.8:c.3061C>G | ENSP00000257430.4:p.Leu1021Val | |
| ENST00000502371.2:c.1414C>G | ||
| ENST00000507379.5:c.3007C>G | ENSP00000423224.1:p.Leu1003Val | |
| ENST00000508376.6:c.3061C>G | ENSP00000427089.2:p.Leu1021Val | |
| ENST00000508624.5:c.*2383C>G | ENSP00000424265.1:n.*2383C>G | |
| ENST00000512211.6:c.3061C>G | ENSP00000423828.2:p.Leu1021Val | |
| ENST00000520401.1:c.230+9683C>G | ||
| NM_000038.5:c.3061C>G | NP_000029.2:p.Leu1021Val | |
| NM_001127510.2:c.3061C>G | NP_001120982.1:p.Leu1021Val | |
| NM_001127511.2:c.3007C>G | NP_001120983.2:p.Leu1003Val | |
| NM_001354895.1:c.3061C>G | NP_001341824.1:p.Leu1021Val | |
| NM_001354896.1:c.3115C>G | NP_001341825.1:p.Leu1039Val | |
| NM_001354897.1:c.3091C>G | NP_001341826.1:p.Leu1031Val | |
| NM_001354898.1:c.2986C>G | NP_001341827.1:p.Leu996Val | |
| NM_001354899.1:c.2977C>G | NP_001341828.1:p.Leu993Val | |
| NM_001354900.1:c.2938C>G | NP_001341829.1:p.Leu980Val | |
| NM_001354901.1:c.2884C>G | NP_001341830.1:p.Leu962Val | |
| NM_001354902.1:c.2788C>G | NP_001341831.1:p.Leu930Val | |
| NM_001354903.1:c.2758C>G | NP_001341832.1:p.Leu920Val | |
| NM_001354904.1:c.2683C>G | NP_001341833.1:p.Leu895Val | |
| NM_001354905.1:c.2581C>G | NP_001341834.1:p.Leu861Val | |
| NM_001354906.1:c.2212C>G | NP_001341835.1:p.Leu738Val | |
| NM_000038.6:c.3061C>G MANE Select | NP_000029.2:p.Leu1021Val | |
| NM_001127510.3:c.3061C>G | NP_001120982.1:p.Leu1021Val | |
| NM_001127511.3:c.3007C>G | NP_001120983.2:p.Leu1003Val | |
| NM_001354895.2:c.3061C>G | NP_001341824.1:p.Leu1021Val | |
| NM_001354896.2:c.3115C>G | NP_001341825.1:p.Leu1039Val | |
| NM_001354897.2:c.3091C>G | NP_001341826.1:p.Leu1031Val | |
| NM_001354898.2:c.2986C>G | NP_001341827.1:p.Leu996Val | |
| NM_001354899.2:c.2977C>G | NP_001341828.1:p.Leu993Val | |
| NM_001354900.2:c.2938C>G | NP_001341829.1:p.Leu980Val | |
| NM_001354901.2:c.2884C>G | NP_001341830.1:p.Leu962Val | |
| NM_001354902.2:c.2788C>G | NP_001341831.1:p.Leu930Val | |
| NM_001354903.2:c.2758C>G | NP_001341832.1:p.Leu920Val | |
| NM_001354904.2:c.2683C>G | NP_001341833.1:p.Leu895Val | |
| NM_001354905.2:c.2581C>G | NP_001341834.1:p.Leu861Val | |
| NM_001354906.2:c.2212C>G | NP_001341835.1:p.Leu738Val |