Linked Data
MyVariant Identifiers:
chr6:g.121768614C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.121447468C>A , CM000668.2:g.121447468C>A | GRCh38 |
| NC_000006.11:g.121768614C>A , CM000668.1:g.121768614C>A | GRCh37 |
| NC_000006.10:g.121810313C>A | NCBI36 |
| NG_008308.1:g.16870C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282561.4:c.621C>A MANE Select | ENSP00000282561.3:p.Thr207= | |
| ENST00000647564.1:c.621C>A | ENSP00000497565.1:p.Thr207= | |
| ENST00000649003.1:c.621C>A | ENSP00000497283.1:p.Thr207= | |
| ENST00000650427.1:c.621C>A | ENSP00000497367.1:p.Thr207= | |
| ENST00000282561.3:c.621C>A | ENSP00000282561.3:p.Thr207= | |
| NM_000165.4:c.621C>A | NP_000156.1:p.Thr207= | |
| NM_000165.5:c.621C>A MANE Select | NP_000156.1:p.Thr207= |