Linked Data
MyVariant Identifiers:
chr20:g.44639604G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46010965G>T , CM000682.2:g.46010965G>T | GRCh38 |
| NC_000020.10:g.44639604G>T , CM000682.1:g.44639604G>T | GRCh37 |
| NC_000020.9:g.44073011G>T | NCBI36 |
| NG_011468.1:g.7058G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.564G>T MANE Select | ENSP00000361405.3:p.Leu188= | |
| NM_004994.2:c.564G>T | NP_004985.2:p.Leu188= | |
| NM_004994.3:c.564G>T MANE Select | NP_004985.2:p.Leu188= |