Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1986039G>A , CM000678.2:g.1986039G>A | GRCh38 |
| NC_000016.9:g.2036040G>A , CM000678.1:g.2036040G>A | GRCh37 |
| NC_000016.8:g.1976041G>A | NCBI36 |
| NG_016288.1:g.6891G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.*11G>A | ENSP00000455885.1:n.*11G>A | |
| ENST00000248114.7:c.*11G>A MANE Select | ENSP00000248114.6:n.*11G>A | |
| ENST00000248114.6:c.*11G>A | ENSP00000248114.6:n.*11G>A | |
| ENST00000565658.1:n.786G>A | ||
| ENST00000567719.1:c.*11G>A | ENSP00000455885.1:n.*11G>A | |
| ENST00000569451.1:c.*102G>A | ENSP00000456432.1:n.*102G>A | |
| NM_005262.2:c.*11G>A | NP_005253.3:n.*11G>A | |
| NM_005262.3:c.*11G>A MANE Select | NP_005253.3:n.*11G>A |