Linked Data
MyVariant Identifiers:
chr17:g.4925668C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.5022373C>T , CM000679.2:g.5022373C>T | GRCh38 |
| NC_000017.10:g.4925668C>T , CM000679.1:g.4925668C>T | GRCh37 |
| NC_000017.9:g.4866392C>T | NCBI36 |
| NG_034137.1:g.29426C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320785.10:c.2292C>T MANE Select | ENSP00000320821.5:p.Phe764= | |
| ENST00000320785.9:c.2292C>T | ENSP00000320821.5:p.Phe764= | |
| NM_006612.5:c.2292C>T | NP_006603.2:p.Phe764= | |
| XM_005256424.1:c.2292C>T | XP_005256481.1:p.Phe764= | |
| XM_005256424.2:c.2292C>T | XP_005256481.1:p.Phe764= | |
| NM_006612.6:c.2292C>T MANE Select | NP_006603.2:p.Phe764= |