Linked Data
MyVariant Identifiers:
chr15:g.75042112C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74749771C>T , CM000677.2:g.74749771C>T | GRCh38 |
| NC_000015.9:g.75042112C>T , CM000677.1:g.75042112C>T | GRCh37 |
| NC_000015.8:g.72829165C>T | NCBI36 |
| NG_008431.1:g.32230C>T | |
| NG_008431.2:g.32230C>T | |
| NG_061543.1:g.5927C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343932.5:c.33C>T MANE Select | ENSP00000342007.4:p.Ala11= | |
| ENST00000343932.4:c.33C>T | ENSP00000342007.4:p.Ala11= | |
| NM_000761.4:c.33C>T | NP_000752.2:p.Ala11= | |
| NM_000761.5:c.33C>T MANE Select | NP_000752.2:p.Ala11= |