Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12857652G>C , CM000686.2:g.12857652G>C | GRCh38 |
| NC_000024.9:g.14969577G>C , CM000686.1:g.14969577G>C | GRCh37 |
| NC_000024.8:g.13478971G>C | NCBI36 |
| NG_008311.1:g.161418G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651177.1:c.7521G>C | ENSP00000498372.1:p.Gln2507His | |
| ENST00000338981.7:c.7521G>C MANE Select | ENSP00000342812.3:p.Gln2507His | |
| ENST00000426564.6:n.7548G>C | ||
| ENST00000453031.1:c.566G>C | ||
| ENST00000471409.1:n.840G>C | ||
| NM_004654.3:c.7521G>C | NP_004645.2:p.Gln2507His | |
| XM_011531469.1:c.7521G>C | XP_011529771.1:p.Gln2507His | |
| XM_011531470.1:c.7287G>C | XP_011529772.1:p.Gln2429His | |
| XM_017030078.2:c.7536G>C | XP_016885567.1:p.Gln2512His | |
| NM_004654.4:c.7521G>C MANE Select | NP_004645.2:p.Gln2507His |