Linked Data
MyVariant Identifiers:
chr6:g.132211483T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131890343T>C , CM000668.2:g.131890343T>C | GRCh38 |
| NC_000006.11:g.132211483T>C , CM000668.1:g.132211483T>C | GRCh37 |
| NC_000006.10:g.132253176T>C | NCBI36 |
| NG_008206.1:g.87328T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684674.1:n.1041T>C | ||
| ENST00000647893.1:c.2610T>C MANE Select | ENSP00000498074.1:p.His870= | |
| ENST00000360971.6:c.2610T>C | ENSP00000354238.2:p.His870= | |
| ENST00000513998.5:c.*1447T>C | ENSP00000422424.1:n.*1447T>C | |
| NM_006208.2:c.2610T>C | NP_006199.2:p.His870= | |
| XM_011535896.1:c.1500T>C | XP_011534198.1:p.His500= | |
| NM_006208.3:c.2610T>C MANE Select | NP_006199.2:p.His870= |