Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.110060889C>T , CM000663.2:g.110060889C>T | GRCh38 |
| NC_000001.10:g.110603511C>T , CM000663.1:g.110603511C>T | GRCh37 |
| NC_000001.9:g.110405034C>T | NCBI36 |
| NG_012039.1:g.14812G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647563.2:c.876G>A (ALX3) MANE Select | ENSP00000497310.1:p.Ala292= | |
| ENST00000649954.1:c.447G>A (ALX3) | ENSP00000497035.1:p.Ala149= | |
| ENST00000369792.4:c.876G>A (ALX3) | ENSP00000358807.3:p.Ala292= | |
| ENST00000473429.5:n.4213+6087C>T (STRIP1) | ||
| NM_006492.2:c.876G>A (ALX3) | NP_006483.2:p.Ala292= | |
| NM_006492.3:c.876G>A (ALX3) MANE Select | NP_006483.2:p.Ala292= |