Linked Data
ClinVar Variation Id:
2449181
ClinVar RCV Id:
RCV003186939
MyVariant Identifiers:
chr20:g.45355576C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46726937C>T , CM000682.2:g.46726937C>T | GRCh38 |
| NC_000020.10:g.45355576C>T , CM000682.1:g.45355576C>T | GRCh37 |
| NC_000020.9:g.44788983C>T | NCBI36 |
| NG_016284.1:g.22298C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359271.4:c.1362C>T MANE Select | ENSP00000352216.2:p.Phe454= | |
| ENST00000359271.3:c.1362C>T | ENSP00000352216.2:p.Phe454= | |
| NM_030777.3:c.1362C>T | NP_110404.1:p.Phe454= | |
| XM_011529060.1:c.1425C>T | XP_011527362.1:p.Phe475= | |
| XM_011529061.1:c.1371C>T | XP_011527363.1:p.Phe457= | |
| XM_011529062.1:c.1474C>T | XP_011527364.1:p.Gln492Ter | |
| XM_011529063.1:c.1425C>T | XP_011527365.1:p.Phe475= | |
| XM_011529064.1:c.1474C>T | XP_011527366.1:p.Gln492Ter | |
| XM_011529065.1:c.1425C>T | XP_011527367.1:p.Phe475= | |
| XR_936641.1:n.1610C>T | ||
| XM_011529060.2:c.1425C>T | XP_011527362.1:p.Phe475= | |
| XM_011529061.2:c.1371C>T | XP_011527363.1:p.Phe457= | |
| XM_011529062.2:c.1474C>T | XP_011527364.1:p.Gln492Ter | |
| XM_011529063.2:c.1425C>T | XP_011527365.1:p.Phe475= | |
| XM_011529064.2:c.1474C>T | XP_011527366.1:p.Gln492Ter | |
| XM_011529065.2:c.1425C>T | XP_011527367.1:p.Phe475= | |
| XM_017028087.2:c.1362C>T | XP_016883576.1:p.Phe454= | |
| XR_936641.2:n.1597C>T | ||
| NM_030777.4:c.1362C>T MANE Select | NP_110404.1:p.Phe454= |