Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.109137529G>C , CM000671.2:g.109137529G>C | GRCh38 |
| NC_000009.11:g.111899809G>C , CM000671.1:g.111899809G>C | GRCh37 |
| NC_000009.10:g.110939630G>C | NCBI36 |
| NG_051235.1:g.34763C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014334.4:c.808C>G MANE Select | NP_055149.3:p.Gln270Glu |
| ENST00000561981.5:c.808C>G MANE Select | ENSP00000477141.2:p.Gln270Glu |
| NM_014334.2:c.961C>G | NP_055149.2:p.Gln321Glu |
| NM_014334.3:c.961C>G | NP_055149.2:p.Gln321Glu |
| ENST00000561981.2:c.961C>G | ENSP00000477141.1:p.Gln321Glu |
| ENST00000644747.1:c.588C>G | ENSP00000493964.1:n.588C>G |
| XM_011518453.1:c.613C>G | XP_011516755.1:p.Gln205Glu |
| XM_011518454.1:c.613C>G | XP_011516756.1:p.Gln205Glu |
| XM_011518454.3:c.613C>G | XP_011516756.1:p.Gln205Glu |