Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174857T= , CM000674.2:g.21174857T= | GRCh38 |
| NC_000012.11:g.21327791T= , CM000674.1:g.21327791T= | GRCh37 |
| NC_000012.10:g.21219058T= | NCBI36 |
| NG_011745.1:g.48664T= , LRG_1022:g.48664T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.359+148T= MANE Select | ENSP00000256958.2:n.359+148T= | |
| ENST00000256958.2:c.359+148T= | ENSP00000256958.2:n.359+148T= | |
| ENST00000543498.5:c.426-1919T= | ||
| NM_006446.4:c.359+148T= , LRG_1022t1:c.359+148T= | NP_006437.3:n.359+148T= | |
| NM_006446.5:c.359+148T= MANE Select | NP_006437.3:n.359+148T= |