Linked Data
dbSNP Id:
rs121908168
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.110064634G>C , CM000663.2:g.110064634G>C | GRCh38 |
| NC_000001.10:g.110607256G>C , CM000663.1:g.110607256G>C | GRCh37 |
| NC_000001.9:g.110408779G>C | NCBI36 |
| NG_012039.1:g.11067C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647563.2:c.547C>G (ALX3) MANE Select | ENSP00000497310.1:p.Arg183Gly | |
| ENST00000649954.1:c.118C>G (ALX3) | ENSP00000497035.1:p.Arg40Gly | |
| ENST00000369792.4:c.547C>G (ALX3) | ENSP00000358807.3:p.Arg183Gly | |
| ENST00000473429.5:n.4214-7821G>C (STRIP1) | ||
| NM_006492.2:c.547C>G (ALX3) | NP_006483.2:p.Arg183Gly | |
| NM_006492.3:c.547C>G (ALX3) MANE Select | NP_006483.2:p.Arg183Gly |