Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2324396C>T , CM000678.2:g.2324396C>T | GRCh38 |
| NC_000016.9:g.2374397C>T , CM000678.1:g.2374397C>T | GRCh37 |
| NC_000016.8:g.2314398C>T | NCBI36 |
| NG_011790.1:g.21351G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001089.3:c.447+8G>A MANE Select | NP_001080.2:n.447+8G>A |
| ENST00000301732.10:c.447+8G>A MANE Select | ENSP00000301732.5:n.447+8G>A |
| NM_001089.2:c.447+8G>A | NP_001080.2:n.447+8G>A |
| ENST00000301732.9:c.447+8G>A | ENSP00000301732.5:n.447+8G>A |
| ENST00000382381.7:c.447+8G>A | ENSP00000371818.3:n.447+8G>A |
| ENST00000563623.5:n.1010+8G>A | |
| ENST00000567910.1:c.447+8G>A | ENSP00000454397.1:n.447+8G>A |