Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110307909G>T , CM000675.2:g.110307909G>T | GRCh38 |
| NC_000013.10:g.110960256G>T , CM000675.1:g.110960256G>T | GRCh37 |
| NC_000013.9:g.109758257G>T | NCBI36 |
| NG_011544.2:g.4241C>A | |
| NG_032137.1:g.5626G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360467.7:c.6G>T MANE Select | ENSP00000353654.5:p.Gly2= | |
| ENST00000400163.7:c.6G>T | ENSP00000383027.3:p.Gly2= | |
| ENST00000649101.1:c.6G>T | ENSP00000497869.1:p.Gly2= | |
| ENST00000650540.1:c.6G>T | ENSP00000497878.1:p.Gly2= | |
| ENST00000360467.5:c.6G>T | ENSP00000353654.5:p.Gly2= | |
| ENST00000400163.6:c.6G>T | ENSP00000383027.2:p.Gly2= | |
| ENST00000480771.5:n.312G>T | ||
| NM_001846.2:c.6G>T | NP_001837.2:p.Gly2= | |
| NM_001846.3:c.6G>T | NP_001837.2:p.Gly2= | |
| NM_001846.4:c.6G>T MANE Select | NP_001837.2:p.Gly2= |