Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5044933C>A , CM000674.2:g.5044933C>A | GRCh38 |
| NC_000012.11:g.5154099C>A , CM000674.1:g.5154099C>A | GRCh37 |
| NC_000012.10:g.5024360C>A | NCBI36 |
| NG_012198.1:g.6015C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.786C>A MANE Select | ENSP00000252321.3:p.Ile262= | |
| ENST00000252321.4:c.786C>A | ENSP00000252321.3:p.Ile262= | |
| NM_002234.3:c.786C>A | NP_002225.2:p.Ile262= | |
| NM_002234.4:c.786C>A MANE Select | NP_002225.2:p.Ile262= |