Linked Data
MyVariant Identifiers:
chr20:g.10639342A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658694A>T , CM000682.2:g.10658694A>T | GRCh38 |
| NC_000020.10:g.10639342A>T , CM000682.1:g.10639342A>T | GRCh37 |
| NC_000020.9:g.10587342A>T | NCBI36 |
| NG_007496.1:g.20353T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.468T>A MANE Select | ENSP00000254958.4:p.Ser156= | |
| ENST00000254958.9:c.468T>A | ENSP00000254958.4:p.Ser156= | |
| ENST00000423891.6:n.334T>A | ||
| NM_000214.2:c.468T>A | NP_000205.1:p.Ser156= | |
| NM_000214.3:c.468T>A MANE Select | NP_000205.1:p.Ser156= |