Linked Data
MyVariant Identifiers:
chr20:g.44638693C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46010054C>G , CM000682.2:g.46010054C>G | GRCh38 |
| NC_000020.10:g.44638693C>G , CM000682.1:g.44638693C>G | GRCh37 |
| NC_000020.9:g.44072100C>G | NCBI36 |
| NG_011468.1:g.6147C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000372330.3:c.327C>G MANE Select | ENSP00000361405.3:p.Thr109= | |
| NM_004994.2:c.327C>G | NP_004985.2:p.Thr109= | |
| NM_004994.3:c.327C>G MANE Select | NP_004985.2:p.Thr109= |