Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12812682C= , CM000686.2:g.12812682C= | GRCh38 |
| NC_000024.9:g.14924617C= , CM000686.1:g.14924617C= | GRCh37 |
| NC_000024.8:g.13434011C= | NCBI36 |
| NG_008311.1:g.116458C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004654.4:c.4387-148C= MANE Select | NP_004645.2:n.4387-148C= |
| ENST00000338981.7:c.4387-148C= MANE Select | ENSP00000342812.3:n.4387-148C= |
| NM_004654.3:c.4387-148C= | NP_004645.2:n.4387-148C= |
| ENST00000426564.6:n.4399-148C= | |
| ENST00000651177.1:c.4387-148C= | ENSP00000498372.1:n.4387-148C= |
| XM_011531469.1:c.4387-148C= | XP_011529771.1:n.4387-148C= |
| XM_011531470.1:c.4153-148C= | XP_011529772.1:n.4153-148C= |
| XM_017030078.2:c.4402-148C= | XP_016885567.1:n.4402-148C= |