Linked Data
MyVariant Identifiers:
chr6:g.132211561T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131890421T>A , CM000668.2:g.131890421T>A | GRCh38 |
| NC_000006.11:g.132211561T>A , CM000668.1:g.132211561T>A | GRCh37 |
| NC_000006.10:g.132253254T>A | NCBI36 |
| NG_008206.1:g.87406T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684674.1:n.1119T>A | ||
| ENST00000647893.1:c.2688T>A MANE Select | ENSP00000498074.1:p.Thr896= | |
| ENST00000360971.6:c.2688T>A | ENSP00000354238.2:p.Thr896= | |
| ENST00000513998.5:c.*1525T>A | ENSP00000422424.1:n.*1525T>A | |
| NM_006208.2:c.2688T>A | NP_006199.2:p.Thr896= | |
| XM_011535896.1:c.1578T>A | XP_011534198.1:p.Thr526= | |
| NM_006208.3:c.2688T>A MANE Select | NP_006199.2:p.Thr896= |