Linked Data
MyVariant Identifiers:
chr1:g.101005383G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.100539827G>T , CM000663.2:g.100539827G>T | GRCh38 |
| NC_000001.10:g.101005383G>T , CM000663.1:g.101005383G>T | GRCh37 |
| NC_000001.9:g.100777971G>T | NCBI36 |
| NG_053134.1:g.6656G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000315033.5:c.861G>T MANE Select | ENSP00000314223.4:p.Leu287= | |
| ENST00000315033.4:c.861G>T | ENSP00000314223.4:p.Leu287= | |
| NM_022049.2:c.861G>T | NP_071332.2:p.Leu287= | |
| NM_022049.3:c.861G>T MANE Select | NP_071332.2:p.Leu287= |