Linked Data
MyVariant Identifiers:
chr17:g.6683814T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6780495T>C , CM000679.2:g.6780495T>C | GRCh38 |
| NC_000017.10:g.6683814T>C , CM000679.1:g.6683814T>C | GRCh37 |
| NC_000017.9:g.6624538T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000321535.5:c.627T>C MANE Select | ENSP00000321386.4:p.Ala209= | |
| ENST00000321535.4:c.627T>C | ENSP00000321386.4:p.Ala209= | |
| NM_153230.2:c.627T>C | NP_694962.1:p.Ala209= | |
| XM_011523697.1:c.627T>C | XP_011521999.1:p.Ala209= | |
| XR_243544.3:n.805T>C | ||
| NM_153230.3:c.627T>C MANE Select | NP_694962.1:p.Ala209= |