Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.110064638A>G , CM000663.2:g.110064638A>G | GRCh38 |
| NC_000001.10:g.110607260A>G , CM000663.1:g.110607260A>G | GRCh37 |
| NC_000001.9:g.110408783A>G | NCBI36 |
| NG_012039.1:g.11063T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647563.2:c.543T>C (ALX3) MANE Select | ENSP00000497310.1:p.Tyr181= | |
| ENST00000649954.1:c.114T>C (ALX3) | ENSP00000497035.1:p.Tyr38= | |
| ENST00000369792.4:c.543T>C (ALX3) | ENSP00000358807.3:p.Tyr181= | |
| ENST00000473429.5:n.4214-7817A>G (STRIP1) | ||
| NM_006492.2:c.543T>C (ALX3) | NP_006483.2:p.Tyr181= | |
| NM_006492.3:c.543T>C (ALX3) MANE Select | NP_006483.2:p.Tyr181= |