Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33668994T>A , CM000668.2:g.33668994T>A | GRCh38 |
| NC_000006.11:g.33636771T>A , CM000668.1:g.33636771T>A | GRCh37 |
| NC_000006.10:g.33744749T>A | NCBI36 |
| NG_027729.1:g.52616T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000605930.3:c.2027T>A MANE Select | ENSP00000475177.1:p.Met676Lys | |
| ENST00000374316.9:c.2027T>A | ENSP00000363435.4:p.Met676Lys | |
| ENST00000605930.2:c.2027T>A | ENSP00000475177.1:p.Met676Lys | |
| NM_002224.3:c.2027T>A | NP_002215.2:p.Met676Lys | |
| XM_011514576.1:c.2096T>A | XP_011512878.1:p.Met699Lys | |
| XM_011514577.1:c.1844T>A | XP_011512879.1:p.Met615Lys | |
| XM_011514577.3:c.1844T>A | XP_011512879.1:p.Met615Lys | |
| XM_017010832.1:c.2027T>A | XP_016866321.1:p.Met676Lys | |
| NM_002224.4:c.2027T>A MANE Select | NP_002215.2:p.Met676Lys |