Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129818693C= , CM000671.2:g.129818693C= | GRCh38 |
| NC_000009.11:g.132580972C= , CM000671.1:g.132580972C= | GRCh37 |
| NC_000009.10:g.131620793C= | NCBI36 |
| NG_008049.1:g.10470G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.621-46G= MANE Select | ENSP00000345719.4:n.621-46G= | |
| ENST00000651202.1:c.717-46G= | ENSP00000498222.1:n.717-46G= | |
| ENST00000351698.4:c.621-46G= | ENSP00000345719.4:n.621-46G= | |
| ENST00000473604.2:n.731-46G= | ||
| ENST00000474192.1:n.38-46G= | ||
| NM_000113.2:c.621-46G= | NP_000104.1:n.621-46G= | |
| XR_929731.1:n.781-46G= | ||
| XR_929731.3:n.649-46G= | ||
| NM_000113.3:c.621-46G= MANE Select | NP_000104.1:n.621-46G= |