Linked Data
ClinVar Variation Id:
3069599
ClinVar RCV Id:
RCV004008143
dbSNP Id:
rs140857754
gnomAD v2:
11-2591899-C-T
gnomAD v4:
11-2570669-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2570669C>T , CM000673.2:g.2570669C>T | GRCh38 |
| NC_000011.9:g.2591899C>T , CM000673.1:g.2591899C>T | GRCh37 |
| NC_000011.8:g.2548475C>T | NCBI36 |
| NG_008935.1:g.130679C>T , LRG_287:g.130679C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.258C>T | ENSP00000434560.2:p.Val86= | |
| ENST00000646564.2:c.478-12766C>T | ENSP00000495806.2:n.478-12766C>T | |
| ENST00000155840.12:c.519C>T MANE Select | ENSP00000155840.2:p.Val173= | |
| ENST00000335475.6:c.138C>T | ENSP00000334497.5:p.Val46= | |
| ENST00000646564.1:c.124-12766C>T | ENSP00000495806.1:n.124-12766C>T | |
| ENST00000155840.9:c.519C>T | ENSP00000155840.2:p.Val173= | |
| ENST00000335475.5:c.138C>T | ENSP00000334497.5:p.Val46= | |
| ENST00000496887.6:c.258C>T | ENSP00000434560.1:p.Val86= | |
| NM_000218.2:c.519C>T , LRG_287t1:c.519C>T | NP_000209.2:p.Val173= | |
| NM_181798.1:c.138C>T , LRG_287t2:c.138C>T | NP_861463.1:p.Val46= | |
| NM_000218.3:c.519C>T MANE Select | NP_000209.2:p.Val173= |