Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52517695G= , CM000674.2:g.52517695G= | GRCh38 |
| NC_000012.11:g.52911479G= , CM000674.1:g.52911479G= | GRCh37 |
| NC_000012.10:g.51197746G= | NCBI36 |
| NG_008297.1:g.7765C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000424.4:c.987C= MANE Select | NP_000415.2:p.Asn329= |
| ENST00000252242.9:c.987C= MANE Select | ENSP00000252242.4:p.Asn329= |
| NM_000424.3:c.987C= | NP_000415.2:p.Asn329= |
| ENST00000252242.8:c.987C= | ENSP00000252242.4:p.Asn329= |
| ENST00000547890.5:n.116C= | |
| ENST00000548409.5:c.109C= | |
| ENST00000549511.5:n.194C= | |
| ENST00000551013.1:n.625C= | |
| ENST00000551188.5:c.430C= | |
| ENST00000552629.5:n.1085C= |