Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.184915168T= , CM000664.2:g.184915168T= | GRCh38 |
| NC_000002.11:g.185779895T= , CM000664.1:g.185779895T= | GRCh37 |
| NC_000002.10:g.185488140T= | NCBI36 |
| NG_046950.1:g.321803T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302277.7:c.256-18435T= MANE Select | ENSP00000303252.6:n.256-18435T= | |
| ENST00000302277.6:c.256-18435T= | ENSP00000303252.6:n.256-18435T= | |
| ENST00000613975.1:c.1-18435T= | ENSP00000483032.1:n.1-18435T= | |
| NM_194250.1:c.256-18435T= | NP_919226.1:n.256-18435T= | |
| NM_194250.2:c.256-18435T= MANE Select | NP_919226.1:n.256-18435T= |