Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1986049A>C , CM000678.2:g.1986049A>C | GRCh38 |
| NC_000016.9:g.2036050A>C , CM000678.1:g.2036050A>C | GRCh37 |
| NC_000016.8:g.1976051A>C | NCBI36 |
| NG_016288.1:g.6901A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.*21A>C | ENSP00000455885.1:n.*21A>C | |
| ENST00000248114.7:c.*21A>C MANE Select | ENSP00000248114.6:n.*21A>C | |
| ENST00000248114.6:c.*21A>C | ENSP00000248114.6:n.*21A>C | |
| ENST00000565658.1:n.796A>C | ||
| ENST00000567719.1:c.*21A>C | ENSP00000455885.1:n.*21A>C | |
| ENST00000569451.1:c.*112A>C | ENSP00000456432.1:n.*112A>C | |
| NM_005262.2:c.*21A>C | NP_005253.3:n.*21A>C | |
| NM_005262.3:c.*21A>C MANE Select | NP_005253.3:n.*21A>C |