Linked Data
ClinVar Variation Id:
2950868
ClinVar RCV Id:
RCV003802130
COSMIC:
COSM3363134
MyVariant Identifiers:
chr20:g.10393758G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10413110G>A , CM000682.2:g.10413110G>A | GRCh38 |
| NC_000020.10:g.10393758G>A , CM000682.1:g.10393758G>A | GRCh37 |
| NC_000020.9:g.10341758G>A | NCBI36 |
| NG_009109.1:g.26109C>T | |
| NG_009109.2:g.26109C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651692.1:c.405C>T | ENSP00000498849.1:p.Thr135= | |
| ENST00000652676.1:n.459-410C>T | ||
| ENST00000347364.7:c.405C>T MANE Select | ENSP00000246062.4:p.Thr135= | |
| ENST00000399054.6:c.405C>T | ENSP00000382008.2:p.Thr135= | |
| NM_018848.3:c.405C>T | NP_061336.1:p.Thr135= | |
| NM_170784.2:c.405C>T | NP_740754.1:p.Thr135= | |
| NR_072977.1:n.364-4307C>T | ||
| NR_072977.2:n.347-4307C>T | ||
| NM_170784.3:c.405C>T MANE Select | NP_740754.1:p.Thr135= |