Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.20454904T>C , CM000676.2:g.20454904T>C | GRCh38 |
| NC_000014.8:g.20923063T>C , CM000676.1:g.20923063T>C | GRCh37 |
| NC_000014.7:g.19992903T>C | NCBI36 |
| NG_008718.1:g.4774T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000206542.8:c.-221A>G | ENSP00000206542.4:n.-221A>G | |
| ENST00000556252.1:n.150A>G | ||
| ENST00000556439.1:n.186A>G | ||
| NM_017807.3:c.-221A>G | NP_060277.1:n.-221A>G | |
| XM_011536930.1:c.-282A>G | XP_011535232.1:n.-282A>G |