Linked Data
gnomAD v4:
15-74749765-C-T
COSMIC:
COSM5383830
MyVariant Identifiers:
chr15:g.75042106C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74749765C>T , CM000677.2:g.74749765C>T | GRCh38 |
| NC_000015.9:g.75042106C>T , CM000677.1:g.75042106C>T | GRCh37 |
| NC_000015.8:g.72829159C>T | NCBI36 |
| NG_008431.1:g.32224C>T | |
| NG_008431.2:g.32224C>T | |
| NG_061543.1:g.5921C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343932.5:c.27C>T MANE Select | ENSP00000342007.4:p.Phe9= | |
| ENST00000343932.4:c.27C>T | ENSP00000342007.4:p.Phe9= | |
| NM_000761.4:c.27C>T | NP_000752.2:p.Phe9= | |
| NM_000761.5:c.27C>T MANE Select | NP_000752.2:p.Phe9= |