Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52488428C= , CM000674.2:g.52488428C= | GRCh38 |
| NC_000012.11:g.52882212C= , CM000674.1:g.52882212C= | GRCh37 |
| NC_000012.10:g.51168479C= | NCBI36 |
| NG_008298.1:g.9970G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330722.7:c.1324G= MANE Select | ENSP00000369317.3:p.Ala442= | |
| ENST00000330722.6:c.1324G= | ENSP00000369317.3:p.Ala442= | |
| NM_005554.3:c.1324G= | NP_005545.1:p.Ala442= | |
| NM_005554.4:c.1324G= MANE Select | NP_005545.1:p.Ala442= |