Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.102207401T>C , CM000670.2:g.102207401T>C | GRCh38 |
| NC_000008.10:g.103219629T>C , CM000670.1:g.103219629T>C | GRCh37 |
| NC_000008.9:g.103288805T>C | NCBI36 |
| NG_016617.1:g.36718A>G , LRG_788:g.36718A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251810.8:c.*732A>G MANE Select | ENSP00000251810.3:n.*732A>G | |
| ENST00000251810.7:c.*732A>G | ENSP00000251810.3:n.*732A>G | |
| ENST00000621845.1:c.*732A>G | ENSP00000484318.1:n.*732A>G | |
| NM_001172477.1:c.*732A>G , LRG_788t1:c.*732A>G | NP_001165948.1:n.*732A>G | |
| NM_001172478.1:c.*732A>G | NP_001165949.1:n.*732A>G | |
| NM_015713.4:c.*732A>G , LRG_788t2:c.*732A>G | NP_056528.2:n.*732A>G | |
| NM_001172478.2:c.*732A>G | NP_001165949.1:n.*732A>G | |
| NM_015713.5:c.*732A>G MANE Select | NP_056528.2:n.*732A>G |