Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985797A>T , CM000678.2:g.1985797A>T | GRCh38 |
| NC_000016.9:g.2035798A>T , CM000678.1:g.2035798A>T | GRCh37 |
| NC_000016.8:g.1975799A>T | NCBI36 |
| NG_016288.1:g.6649A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.231-69A>T | ENSP00000455885.1:n.231-69A>T | |
| ENST00000248114.7:c.456-69A>T MANE Select | ENSP00000248114.6:n.456-69A>T | |
| ENST00000248114.6:c.456-69A>T | ENSP00000248114.6:n.456-69A>T | |
| ENST00000565658.1:n.613-69A>T | ||
| ENST00000567719.1:c.231-69A>T | ENSP00000455885.1:n.231-69A>T | |
| ENST00000569451.1:c.259-69A>T | ENSP00000456432.1:n.259-69A>T | |
| NM_005262.2:c.456-69A>T | NP_005253.3:n.456-69A>T | |
| NM_005262.3:c.456-69A>T MANE Select | NP_005253.3:n.456-69A>T |