Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110170508C= , CM000675.2:g.110170508C= | GRCh38 |
| NC_000013.10:g.110822855C= , CM000675.1:g.110822855C= | GRCh37 |
| NC_000013.9:g.109620856C= | NCBI36 |
| NG_011544.2:g.141642G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.3742+39G= MANE Select | ENSP00000364979.4:n.3742+39G= | |
| ENST00000375820.8:c.3742+39G= | ENSP00000364979.4:n.3742+39G= | |
| NM_001845.5:c.3742+39G= | NP_001836.3:n.3742+39G= | |
| XM_011521048.1:c.3550+39G= | XP_011519350.1:n.3550+39G= | |
| XM_011521048.2:c.3550+39G= | XP_011519350.1:n.3550+39G= | |
| NM_001845.6:c.3742+39G= MANE Select | NP_001836.3:n.3742+39G= |