Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35437723G>C , CM000682.2:g.35437723G>C | GRCh38 |
| NC_000020.10:g.34025503G>C , CM000682.1:g.34025503G>C | GRCh37 |
| NC_000020.9:g.33488917G>C | NCBI36 |
| NG_008076.2:g.5497C>G | |
| NG_008076.3:g.22024C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000557.5:c.206C>G MANE Select | NP_000548.2:p.Ala69Gly |
| ENST00000374369.8:c.206C>G MANE Select | ENSP00000363489.3:p.Ala69Gly |
| NM_000557.4:c.206C>G | NP_000548.2:p.Ala69Gly |
| NM_001319138.1:c.206C>G | NP_001306067.1:p.Ala69Gly |
| NM_001319138.2:c.206C>G | NP_001306067.1:p.Ala69Gly |
| ENST00000374369.7:c.206C>G | ENSP00000363489.3:p.Ala69Gly |
| ENST00000374372.1:c.206C>G | ENSP00000363492.1:p.Ala69Gly |
| XM_011529075.1:c.206C>G | XP_011527377.1:p.Ala69Gly |
| XM_011529076.1:c.206C>G | XP_011527378.1:p.Ala69Gly |