Linked Data
ClinVar Variation Id:
2046429
ClinVar RCV Id:
RCV002926600
MyVariant Identifiers:
chr1:g.949681G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1014301G>A , CM000663.2:g.1014301G>A | GRCh38 |
| NC_000001.10:g.949681G>A , CM000663.1:g.949681G>A | GRCh37 |
| NC_000001.9:g.939544G>A | NCBI36 |
| NG_033033.1:g.5835G>A | |
| NG_033033.2:g.18164G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000624697.4:c.297G>A | ENSP00000485643.1:p.Leu99= | |
| ENST00000649529.1:c.321G>A MANE Select | ENSP00000496832.1:p.Leu107= | |
| ENST00000379389.4:c.321G>A | ENSP00000368699.4:p.Leu107= | |
| ENST00000624652.1:c.297G>A | ENSP00000485313.1:p.Leu99= | |
| ENST00000624697.3:c.297G>A | ENSP00000485643.1:p.Leu99= | |
| NM_005101.3:c.321G>A | NP_005092.1:p.Leu107= | |
| NM_005101.4:c.321G>A MANE Select | NP_005092.1:p.Leu107= |