Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118951813G>A , CM000670.2:g.118951813G>A | GRCh38 |
| NC_000008.10:g.119964052G>A , CM000670.1:g.119964052G>A | GRCh37 |
| NC_000008.9:g.120033233G>A | NCBI36 |
| NG_012202.1:g.5332C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002546.4:c.9C>T MANE Select | NP_002537.3:p.Asn3= |
| ENST00000297350.9:c.9C>T MANE Select | ENSP00000297350.4:p.Asn3= |
| NM_002546.3:c.9C>T | NP_002537.3:p.Asn3= |
| ENST00000297350.8:c.9C>T | ENSP00000297350.4:p.Asn3= |
| ENST00000517352.1:c.9C>T | ENSP00000427924.1:p.Asn3= |