Linked Data
MyVariant Identifiers:
chr6:g.132182749T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131861609T>C , CM000668.2:g.131861609T>C | GRCh38 |
| NC_000006.11:g.132182749T>C , CM000668.1:g.132182749T>C | GRCh37 |
| NC_000006.10:g.132224442T>C | NCBI36 |
| NG_008206.1:g.58594T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647893.1:c.930T>C MANE Select | ENSP00000498074.1:p.Ala310= | |
| ENST00000650147.1:c.547T>C | ||
| ENST00000650437.1:c.421T>C | ||
| ENST00000360971.6:c.930T>C | ENSP00000354238.2:p.Ala310= | |
| ENST00000513998.5:c.930T>C | ENSP00000422424.1:p.Ala310= | |
| NM_006208.2:c.930T>C | NP_006199.2:p.Ala310= | |
| NM_006208.3:c.930T>C MANE Select | NP_006199.2:p.Ala310= |