Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.56500729G= , CM000663.2:g.56500729G= | GRCh38 |
| NC_000001.10:g.56966401G= , CM000663.1:g.56966401G= | GRCh37 |
| NC_000001.9:g.56738989G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371250.4:c.811-4053C= MANE Select | ENSP00000360296.3:n.811-4053C= | |
| ENST00000641109.1:c.220-4053C= | ENSP00000493138.1:n.220-4053C= | |
| ENST00000641494.1:c.65-4053C= | ||
| ENST00000642129.1:c.455-4053C= | ||
| ENST00000371250.3:c.811-4053C= | ENSP00000360296.3:n.811-4053C= | |
| ENST00000459962.1:n.1797-4053C= | ||
| ENST00000472957.1:n.296-4053C= | ||
| NM_003713.4:c.811-4053C= | NP_003704.3:n.811-4053C= | |
| NM_003713.5:c.811-4053C= MANE Select | NP_003704.3:n.811-4053C= |