Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19466452T>A , CM000686.2:g.19466452T>A | GRCh38 |
| NC_000024.9:g.21628338T>A , CM000686.1:g.21628338T>A | GRCh37 |
| NC_000024.8:g.20087726T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_002923.2:n.1671+4A>T | |
| NR_033732.1:n.1671+4A>T | |
| ENST00000400605.5:n.1654+4A>T | |
| ENST00000441139.5:n.1671+4A>T | |
| ENST00000513194.1:n.4571A>T | |
| ENST00000650676.1:n.1660+4A>T |