Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.176771G>A , CM000678.2:g.176771G>A | GRCh38 |
| NC_000016.9:g.226770G>A , CM000678.1:g.226770G>A | GRCh37 |
| NC_000016.8:g.166770G>A | NCBI36 |
| NG_000006.1:g.37634G>A | |
| NG_059186.1:g.5121G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000558.5:c.55G>A MANE Select | NP_000549.1:p.Gly19Ser |
| ENST00000320868.9:c.55G>A MANE Select | ENSP00000322421.5:p.Gly19Ser |
| NM_000558.4:c.55G>A | NP_000549.1:p.Gly19Ser |
| ENST00000397797.1:c.-2+9G>A | ENSP00000380899.1:n.-2+9G>A |
| ENST00000472694.1:n.74G>A | |
| ENST00000487791.1:n.24G>A |