Linked Data
MyVariant Identifiers:
chr1:g.109807123C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109264501C>T , CM000663.2:g.109264501C>T | GRCh38 |
| NC_000001.10:g.109807123C>T , CM000663.1:g.109807123C>T | GRCh37 |
| NC_000001.9:g.109608646C>T | NCBI36 |
| NG_052669.1:g.19797C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271332.4:c.5337C>T MANE Select | ENSP00000271332.3:p.Pro1779= | |
| ENST00000271332.3:c.5337C>T | ENSP00000271332.3:p.Pro1779= | |
| NM_001408.2:c.5337C>T | NP_001399.1:p.Pro1779= | |
| XM_005270580.3:c.5337C>T | XP_005270637.1:p.Pro1779= | |
| NM_001408.3:c.5337C>T MANE Select | NP_001399.1:p.Pro1779= |