Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.108631651C>A , CM000674.2:g.108631651C>A | GRCh38 |
| NC_000012.11:g.109025427C>A , CM000674.1:g.109025427C>A | GRCh37 |
| NC_000012.10:g.107549556C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000550948.2:c.-6+2089G>T MANE Select | ENSP00000447752.1:n.-6+2089G>T | |
| ENST00000228463.6:c.43+208G>T | ENSP00000228463.6:n.43+208G>T | |
| ENST00000550948.1:c.-6+2089G>T | ENSP00000447752.1:n.-6+2089G>T | |
| NM_001206609.1:c.43+208G>T | NP_001193538.1:n.43+208G>T | |
| NM_003006.4:c.-6+2089G>T MANE Select | NP_002997.2:n.-6+2089G>T | |
| XM_005269076.2:c.-6+2089G>T | XP_005269133.1:n.-6+2089G>T | |
| XR_945327.1:n.283+2902C>A | ||
| XR_945327.3:n.406+2902C>A | ||
| NM_001206609.2:c.43+208G>T | NP_001193538.1:n.43+208G>T |