Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.72577902A= , CM000671.2:g.72577902A= | GRCh38 |
| NC_000009.11:g.75192818A= , CM000671.1:g.75192818A= | GRCh37 |
| NC_000009.10:g.74382638A= | NCBI36 |
| NG_008213.1:g.61102A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297784.10:c.-427A= MANE Select | ENSP00000297784.6:n.-427A= | |
| ENST00000643676.1:n.307-38466A= | ||
| ENST00000645208.2:c.-427A= | ENSP00000494684.1:n.-427A= | |
| ENST00000650689.1:n.66A= | ||
| ENST00000651183.1:c.-528A= | ENSP00000498723.1:n.-528A= | |
| ENST00000651743.1:n.116A= | ||
| ENST00000297784.9:c.-427A= | ENSP00000297784.5:n.-427A= | |
| ENST00000497073.1:n.115A= | ||
| NM_138691.2:c.-427A= | NP_619636.2:n.-427A= | |
| NM_138691.3:c.-427A= MANE Select | NP_619636.2:n.-427A= |