Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.20389390A= , CM000678.2:g.20389390A= | GRCh38 |
| NC_000016.9:g.20400712A= , CM000678.1:g.20400712A= | GRCh37 |
| NC_000016.8:g.20308213A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302451.9:c.203-4539T= MANE Select | ENSP00000305465.4:n.203-4539T= | |
| ENST00000302451.8:c.203-4539T= | ENSP00000305465.4:n.203-4539T= | |
| ENST00000575561.1:c.203-481T= | ENSP00000459161.1:n.203-481T= | |
| NM_174924.1:c.203-4539T= | NP_777584.1:n.203-4539T= | |
| XM_006721024.1:c.203-4539T= | XP_006721087.1:n.203-4539T= | |
| XM_011545764.1:c.203-4539T= | XP_011544066.1:n.203-4539T= | |
| XM_011545765.1:c.203-4539T= | XP_011544067.1:n.203-4539T= | |
| XR_950754.1:n.457-4539T= | ||
| NM_174924.2:c.203-4539T= MANE Select | NP_777584.1:n.203-4539T= |