Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583055T>G , CM000679.2:g.41583055T>G | GRCh38 |
| NC_000017.10:g.39739307T>G , CM000679.1:g.39739307T>G | GRCh37 |
| NC_000017.9:g.36992833T>G | NCBI36 |
| NG_008624.1:g.8841A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.1321+39A>C MANE Select | ENSP00000167586.6:n.1321+39A>C | |
| ENST00000167586.6:c.1321+39A>C | ENSP00000167586.6:n.1321+39A>C | |
| ENST00000441550.2:n.307A>C | ||
| NM_000526.4:c.1321+39A>C | NP_000517.2:n.1321+39A>C | |
| NM_000526.5:c.1321+39A>C MANE Select | NP_000517.3:n.1321+39A>C |