Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.114785363T>C , CM000671.2:g.114785363T>C | GRCh38 |
| NC_000009.11:g.117547643T>C , CM000671.1:g.117547643T>C | GRCh37 |
| NC_000009.10:g.116587464T>C | NCBI36 |
| NG_011488.2:g.25766A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374045.5:c.*5089A>G MANE Select | ENSP00000363157.3:n.*5089A>G | |
| ENST00000374045.4:c.*5089A>G | ENSP00000363157.3:n.*5089A>G | |
| NM_001204344.1:c.5668A>G | NP_001191273.1:n.5668A>G | |
| NM_005118.3:c.*5089A>G | NP_005109.2:n.*5089A>G | |
| NM_005118.4:c.*5089A>G MANE Select | NP_005109.2:n.*5089A>G |