Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88717172C= , CM000678.2:g.88717172C= | GRCh38 |
| NC_000016.9:g.88783580C= , CM000678.1:g.88783580C= | GRCh37 |
| NC_000016.8:g.87311081C= | NCBI36 |
| NG_042229.1:g.73049G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001142864.4:c.6511G= MANE Select | NP_001136336.2:p.Val2171= |
| ENST00000301015.14:c.6511G= MANE Select | ENSP00000301015.9:p.Val2171= |
| NM_001142864.2:c.6511G= | NP_001136336.2:p.Val2171= |
| NM_001142864.3:c.6511G= | NP_001136336.2:p.Val2171= |
| ENST00000301015.13:c.6511G= | ENSP00000301015.9:p.Val2171= |
| ENST00000327397.8:c.115G= | ENSP00000333704.7:p.Val39= |
| ENST00000419505.5:c.356G= | ENSP00000406358.1:n.356G= |
| ENST00000484567.5:n.1147G= | |
| ENST00000484567.6:n.1570G= | |
| ENST00000495568.7:n.752G= |