Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.110070303G>A , CM000663.2:g.110070303G>A | GRCh38 |
| NC_000001.10:g.110612925G>A , CM000663.1:g.110612925G>A | GRCh37 |
| NC_000001.9:g.110414448G>A | NCBI36 |
| NG_012039.1:g.5398C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006492.3:c.277+33C>T (ALX3) MANE Select | NP_006483.2:n.277+33C>T |
| ENST00000647563.2:c.277+33C>T (ALX3) MANE Select | ENSP00000497310.1:n.277+33C>T |
| NM_006492.2:c.277+33C>T (ALX3) | NP_006483.2:n.277+33C>T |
| ENST00000369792.4:c.277+33C>T (ALX3) | ENSP00000358807.3:n.277+33C>T |
| ENST00000473429.5:n.4214-2152G>A (STRIP1) |