Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115702920C>T , CM000663.2:g.115702920C>T | GRCh38 |
| NC_000001.10:g.116245541C>T , CM000663.1:g.116245541C>T | GRCh37 |
| NC_000001.9:g.116047064C>T | NCBI36 |
| NG_008802.1:g.70886G>A , LRG_404:g.70886G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001232.4:c.1014+1G>A MANE Select | NP_001223.2:n.1014+1G>A |
| ENST00000261448.6:c.1014+1G>A MANE Select | ENSP00000261448.5:n.1014+1G>A |
| NM_001232.3:c.1014+1G>A , LRG_404t1:c.1014+1G>A | NP_001223.2:n.1014+1G>A |
| ENST00000261448.5:c.1014+1G>A | ENSP00000261448.5:n.1014+1G>A |
| ENST00000488931.2:c.*386+1G>A | ENSP00000518226.1:n.*386+1G>A |