Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10649058T>C , CM000682.2:g.10649058T>C | GRCh38 |
| NC_000020.10:g.10629706T>C , CM000682.1:g.10629706T>C | GRCh37 |
| NC_000020.9:g.10577706T>C | NCBI36 |
| NG_007496.1:g.29989A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.1395+3A>G MANE Select | ENSP00000254958.4:n.1395+3A>G | |
| ENST00000617965.2:n.1984+3A>G | ||
| ENST00000254958.9:c.1395+3A>G | ENSP00000254958.4:n.1395+3A>G | |
| ENST00000423891.6:n.1261+3A>G | ||
| ENST00000620743.1:n.117A>G | ||
| ENST00000622545.1:c.172+3A>G | ||
| NM_000214.2:c.1395+3A>G | NP_000205.1:n.1395+3A>G | |
| NM_000214.3:c.1395+3A>G MANE Select | NP_000205.1:n.1395+3A>G |