Linked Data
MyVariant Identifiers:
chr20:g.6077651A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6097004A>T , CM000682.2:g.6097004A>T | GRCh38 |
| NC_000020.10:g.6077651A>T , CM000682.1:g.6077651A>T | GRCh37 |
| NC_000020.9:g.6025651A>T | NCBI36 |
| NG_016213.1:g.31541T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699095.1:c.987T>A | ENSP00000514127.1:p.Ala329= | |
| ENST00000699096.1:n.1449T>A | ||
| ENST00000699097.1:n.157T>A | ||
| ENST00000217289.9:c.987T>A MANE Select | ENSP00000217289.4:p.Ala329= | |
| ENST00000217289.8:c.987T>A | ENSP00000217289.4:p.Ala329= | |
| ENST00000536936.1:c.216T>A | ENSP00000441063.1:p.Ala72= | |
| NM_017671.4:c.987T>A | NP_060141.3:p.Ala329= | |
| XM_024451935.1:c.987T>A | XP_024307703.1:p.Ala329= | |
| NM_017671.5:c.987T>A MANE Select | NP_060141.3:p.Ala329= |