Linked Data
MyVariant Identifiers:
chr20:g.6751055C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6770408C>T , CM000682.2:g.6770408C>T | GRCh38 |
| NC_000020.10:g.6751055C>T , CM000682.1:g.6751055C>T | GRCh37 |
| NC_000020.9:g.6699055C>T | NCBI36 |
| NG_023233.1:g.7311C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378827.5:c.282C>T MANE Select | ENSP00000368104.3:p.Ala94= | |
| ENST00000378827.4:c.282C>T | ENSP00000368104.3:p.Ala94= | |
| NM_001200.2:c.282C>T | NP_001191.1:p.Ala94= | |
| XM_011529323.1:c.-123+1533C>T | XP_011527625.1:n.-123+1533C>T | |
| NM_001200.3:c.282C>T | NP_001191.1:p.Ala94= | |
| NM_001200.4:c.282C>T MANE Select | NP_001191.1:p.Ala94= |