Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.110070432G>C , CM000663.2:g.110070432G>C | GRCh38 |
| NC_000001.10:g.110613054G>C , CM000663.1:g.110613054G>C | GRCh37 |
| NC_000001.9:g.110414577G>C | NCBI36 |
| NG_012039.1:g.5269C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006492.3:c.181C>G (ALX3) MANE Select | NP_006483.2:p.Leu61Val |
| ENST00000647563.2:c.181C>G (ALX3) MANE Select | ENSP00000497310.1:p.Leu61Val |
| NM_006492.2:c.181C>G (ALX3) | NP_006483.2:p.Leu61Val |
| ENST00000369792.4:c.181C>G (ALX3) | ENSP00000358807.3:p.Leu61Val |
| ENST00000473429.5:n.4214-2023G>C (STRIP1) |