Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.38683063A= , CM000668.2:g.38683063A= | GRCh38 |
| NC_000006.11:g.38650839A= , CM000668.1:g.38650839A= | GRCh37 |
| NC_000006.10:g.38758817A= | NCBI36 |
| NG_012074.1:g.25114T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373365.5:c.309-188T= MANE Select | ENSP00000362463.3:n.309-188T= | |
| ENST00000373365.4:c.309-188T= | ENSP00000362463.3:n.309-188T= | |
| ENST00000470973.1:n.153T= | ||
| NM_006708.2:c.309-188T= | NP_006699.2:n.309-188T= | |
| NM_006708.3:c.309-188T= MANE Select | NP_006699.2:n.309-188T= |