Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.62528618T>C , CM000672.2:g.62528618T>C | GRCh38 |
| NC_000010.10:g.64288377T>C , CM000672.1:g.64288377T>C | GRCh37 |
| NC_000010.9:g.63958383T>C | NCBI36 |
| NG_021209.1:g.159462T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647733.1:c.981+68821T>C | ENSP00000502188.1:n.981+68821T>C | |
| ENST00000395251.5:c.-185+8021T>C | ENSP00000378672.1:n.-185+8021T>C | |
| ENST00000410046.7:c.981+68821T>C | ENSP00000387091.3:n.981+68821T>C | |
| NM_199451.2:c.981+68821T>C | NP_955523.1:n.981+68821T>C | |
| NM_199452.3:c.-185+8021T>C | NP_955524.3:n.-185+8021T>C | |
| XM_017015937.2:c.982-15591T>C | XP_016871426.1:n.982-15591T>C | |
| NM_199451.3:c.981+68821T>C | NP_955523.1:n.981+68821T>C |