Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14076952T>A , CM000673.2:g.14076952T>A | GRCh38 |
| NC_000011.9:g.14098499T>A , CM000673.1:g.14098499T>A | GRCh37 |
| NC_000011.8:g.14055075T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000576479.4:c.553+1534T>A MANE Select | ENSP00000460236.1:n.553+1534T>A | |
| ENST00000576479.3:c.553+1534T>A | ENSP00000460236.1:n.553+1534T>A | |
| NM_006108.3:c.553+1534T>A | NP_006099.2:n.553+1534T>A | |
| NM_006108.4:c.553+1534T>A MANE Select | NP_006099.2:n.553+1534T>A |