Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10644822T= , CM000682.2:g.10644822T= | GRCh38 |
| NC_000020.10:g.10625470T= , CM000682.1:g.10625470T= | GRCh37 |
| NC_000020.9:g.10573470T= | NCBI36 |
| NG_007496.1:g.34225A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000254958.10:c.2344+41A= MANE Select | ENSP00000254958.4:n.2344+41A= | |
| ENST00000617965.2:n.2933+41A= | ||
| ENST00000254958.9:c.2344+41A= | ENSP00000254958.4:n.2344+41A= | |
| ENST00000423891.6:n.2210+41A= | ||
| ENST00000488480.2:n.782A= | ||
| NM_000214.2:c.2344+41A= | NP_000205.1:n.2344+41A= | |
| NM_000214.3:c.2344+41A= MANE Select | NP_000205.1:n.2344+41A= |