Linked Data
ClinVar Variation Id:
2144905
ClinVar RCV Id:
RCV003063175
dbSNP Id:
rs1171271917
gnomAD v2:
9-6556281-G-C
gnomAD v4:
9-6556281-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6556281G>C , CM000671.2:g.6556281G>C | GRCh38 |
| NC_000009.11:g.6556281G>C , CM000671.1:g.6556281G>C | GRCh37 |
| NC_000009.10:g.6546281G>C | NCBI36 |
| NG_016397.1:g.94412C>G , LRG_643:g.94412C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000321612.8:c.2074C>G MANE Select | ENSP00000370737.4:p.Leu692Val | |
| ENST00000638233.1:n.509C>G | ||
| ENST00000638661.1:c.274C>G | ENSP00000491369.1:p.Leu92Val | |
| ENST00000638694.1:n.261C>G | ||
| ENST00000639318.1:c.274C>G | ENSP00000491932.1:p.Leu92Val | |
| ENST00000639364.1:n.1774C>G | ||
| ENST00000639443.1:n.1642C>G | ||
| ENST00000639954.1:n.1782C>G | ||
| ENST00000640505.1:n.313C>G | ||
| ENST00000321612.6:c.2074C>G | ENSP00000370737.3:p.Leu692Val | |
| NM_000170.2:c.2074C>G , LRG_643t1:c.2074C>G | NP_000161.2:p.Leu692Val | |
| NM_000170.3:c.2074C>G MANE Select | NP_000161.2:p.Leu692Val |