Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.756995G>A , CM000669.2:g.756995G>A | GRCh38 |
| NC_000007.13:g.796632G>A , CM000669.1:g.796632G>A | GRCh37 |
| NC_000007.12:g.763158G>A | NCBI36 |
| NG_033137.1:g.35295G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017802.4:c.1470+1G>A MANE Select | NP_060272.3:n.1470+1G>A |
| ENST00000297440.11:c.1470+1G>A MANE Select | ENSP00000297440.6:n.1470+1G>A |
| NM_017802.3:c.1470+1G>A | NP_060272.3:n.1470+1G>A |
| NR_075098.1:n.1428+1G>A | |
| NR_075098.2:n.1430+1G>A | |
| ENST00000297440.10:c.1470+1G>A | ENSP00000297440.6:n.1470+1G>A |
| ENST00000440747.5:c.874+1G>A | |
| XM_024446813.1:c.1470+1G>A | XP_024302581.1:n.1470+1G>A |
| XM_024446814.1:c.864+1G>A | XP_024302582.1:n.864+1G>A |