Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120727006A>T , CM000674.2:g.120727006A>T | GRCh38 |
| NC_000012.11:g.121164809A>T , CM000674.1:g.121164809A>T | GRCh37 |
| NC_000012.10:g.119649192A>T | NCBI36 |
| NG_007991.1:g.6239A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242592.9:c.47-20A>T MANE Select | ENSP00000242592.4:n.47-20A>T | |
| ENST00000242592.8:c.47-20A>T | ENSP00000242592.4:n.47-20A>T | |
| ENST00000411593.2:c.47-20A>T | ENSP00000401045.2:n.47-20A>T | |
| ENST00000539690.1:n.159-20A>T | ||
| NM_000017.3:c.47-20A>T | NP_000008.1:n.47-20A>T | |
| NM_001302554.1:c.47-20A>T | NP_001289483.1:n.47-20A>T | |
| NM_000017.4:c.47-20A>T MANE Select | NP_000008.1:n.47-20A>T | |
| NM_001302554.2:c.47-20A>T | NP_001289483.1:n.47-20A>T |