Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31580866G>T , CM000664.2:g.31580866G>T | GRCh38 |
| NC_000002.11:g.31805935G>T , CM000664.1:g.31805935G>T | GRCh37 |
| NC_000002.10:g.31659439G>T | NCBI36 |
| NG_008365.1:g.5106C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000348.4:c.35C>A MANE Select | NP_000339.2:p.Ala12Glu |
| ENST00000622030.2:c.35C>A MANE Select | ENSP00000477587.1:p.Ala12Glu |
| NM_000348.3:c.35C>A | NP_000339.2:p.Ala12Glu |
| ENST00000622030.1:c.35C>A | ENSP00000477587.1:p.Ala12Glu |
| XM_011533068.1:c.35C>A | XP_011531370.1:p.Ala12Glu |
| XM_011533070.1:c.27-47100C>A | XP_011531372.1:n.27-47100C>A |
| XM_011533071.1:c.27-47100C>A | XP_011531373.1:n.27-47100C>A |
| XM_011533072.1:c.27-47100C>A | XP_011531374.1:n.27-47100C>A |
| XM_011533072.2:c.27-47100C>A | XP_011531374.1:n.27-47100C>A |