Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152805935T>C , CM000663.2:g.152805935T>C | GRCh38 |
| NC_000001.10:g.152778411T>C , CM000663.1:g.152778411T>C | GRCh37 |
| NC_000001.9:g.151045035T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000607093.2:c.-20-437A>G MANE Select | ENSP00000475270.1:n.-20-437A>G | |
| ENST00000606576.1:c.-20-437A>G | ENSP00000476034.1:n.-20-437A>G | |
| NM_001276331.1:c.-20-437A>G | NP_001263260.1:n.-20-437A>G | |
| NM_178351.3:c.-20-437A>G | NP_848128.1:n.-20-437A>G | |
| NM_001276331.2:c.-20-437A>G | NP_001263260.1:n.-20-437A>G | |
| NM_178351.4:c.-20-437A>G MANE Select | NP_848128.1:n.-20-437A>G |