Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6709668G>C , CM000681.2:g.6709668G>C | GRCh38 |
| NC_000019.9:g.6709679G>C , CM000681.1:g.6709679G>C | GRCh37 |
| NC_000019.8:g.6660679G>C | NCBI36 |
| NG_009557.1:g.15984C>G , LRG_27:g.15984C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695652.1:c.1722+16C>G | ENSP00000512083.1:n.1722+16C>G | |
| ENST00000695654.1:c.969+16C>G | ENSP00000512085.1:n.969+16C>G | |
| ENST00000695655.1:c.786+16C>G | ENSP00000512086.1:n.786+16C>G | |
| ENST00000695692.1:n.1209+16C>G | ||
| ENST00000245907.11:c.1845+16C>G MANE Select | ENSP00000245907.4:n.1845+16C>G | |
| ENST00000245907.10:c.1845+16C>G | ENSP00000245907.4:n.1845+16C>G | |
| NM_000064.3:c.1845+16C>G | NP_000055.2:n.1845+16C>G | |
| NM_000064.4:c.1845+16C>G MANE Select | NP_000055.2:n.1845+16C>G |