Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75008922T= , CM000676.2:g.75008922T= | GRCh38 |
| NC_000014.8:g.75475625T= , CM000676.1:g.75475625T= | GRCh37 |
| NC_000014.7:g.74545378T= | NCBI36 |
| NG_013333.1:g.11014T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266126.10:c.899-109T= MANE Select | ENSP00000266126.5:n.899-109T= | |
| ENST00000266126.9:c.899-109T= | ENSP00000266126.5:n.899-109T= | |
| ENST00000556668.1:n.479-109T= | ||
| NM_014239.3:c.899-109T= | NP_055054.1:n.899-109T= | |
| NM_014239.4:c.899-109T= MANE Select | NP_055054.1:n.899-109T= |