Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206802774T= , CM000663.2:g.206802774T= | GRCh38 |
| NC_000001.10:g.206976119T= , CM000663.1:g.206976119T= | GRCh37 |
| NC_000001.9:g.205042742T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_153758.5:c.-3+3768T= MANE Select | NP_715639.2:n.-3+3768T= |
| ENST00000659997.3:c.-3+3768T= MANE Select | ENSP00000499459.2:n.-3+3768T= |
| NM_001393490.1:c.-3+3768T= | NP_001380419.1:n.-3+3768T= |
| NM_153758.2:c.112+3768T= | NP_715639.1:n.112+3768T= |
| NM_153758.3:c.112+3768T= | NP_715639.1:n.112+3768T= |
| ENST00000340758.6:c.112+3768T= | ENSP00000343000.2:n.112+3768T= |
| ENST00000656872.2:c.-3+3768T= | ENSP00000499487.2:n.-3+3768T= |
| ENST00000659997.2:c.-3+3768T= | ENSP00000499459.2:n.-3+3768T= |
| ENST00000662320.1:n.213+3768T= |