Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.15415414T>A , CM000685.2:g.15415414T>A | GRCh38 |
| NC_000023.10:g.15433536T>A , CM000685.1:g.15433536T>A | GRCh37 |
| NC_000023.9:g.15343457T>A | NCBI36 |
| NG_012549.1:g.82929A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001018109.3:c.566-7864A>T MANE Select | NP_001018119.1:n.566-7864A>T |
| ENST00000380420.10:c.566-7864A>T MANE Select | ENSP00000369785.5:n.566-7864A>T |
| NM_001018109.2:c.566-7864A>T | NP_001018119.1:n.566-7864A>T |
| NM_003662.3:c.566-7864A>T | NP_003653.1:n.566-7864A>T |
| NM_003662.4:c.566-7864A>T | NP_003653.1:n.566-7864A>T |
| NR_037859.2:n.618-7864A>T | |
| ENST00000380420.9:c.566-7864A>T | ENSP00000369785.5:n.566-7864A>T |
| ENST00000380421.3:c.566-7864A>T | ENSP00000369786.3:n.566-7864A>T |