Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115726986A>T , CM000663.2:g.115726986A>T | GRCh38 |
| NC_000001.10:g.116269607A>T , CM000663.1:g.116269607A>T | GRCh37 |
| NC_000001.9:g.116071130A>T | NCBI36 |
| NG_008802.1:g.46820T>A , LRG_404:g.46820T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001232.4:c.737+6T>A MANE Select | NP_001223.2:n.737+6T>A |
| ENST00000261448.6:c.737+6T>A MANE Select | ENSP00000261448.5:n.737+6T>A |
| NM_001232.3:c.737+6T>A , LRG_404t1:c.737+6T>A | NP_001223.2:n.737+6T>A |
| ENST00000261448.5:c.737+6T>A | ENSP00000261448.5:n.737+6T>A |
| ENST00000488931.2:c.*109+6T>A | ENSP00000518226.1:n.*109+6T>A |