Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32444056C>G , CM000668.2:g.32444056C>G | GRCh38 |
| NC_000006.11:g.32411833C>G , CM000668.1:g.32411833C>G | GRCh37 |
| NC_000006.10:g.32519811C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019111.5:c.*11+135C>G MANE Select | NP_061984.2:n.*11+135C>G |
| ENST00000395388.7:c.*11+135C>G MANE Select | ENSP00000378786.2:n.*11+135C>G |
| NM_019111.4:c.*11+135C>G | NP_061984.2:n.*11+135C>G |
| ENST00000374982.5:c.*11+135C>G | ENSP00000364121.5:n.*11+135C>G |
| ENST00000395388.6:c.*11+135C>G | ENSP00000378786.2:n.*11+135C>G |