Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110161189C>A , CM000675.2:g.110161189C>A | GRCh38 |
| NC_000013.10:g.110813536C>A , CM000675.1:g.110813536C>A | GRCh37 |
| NC_000013.9:g.109611537C>A | NCBI36 |
| NG_011544.2:g.150961G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001845.6:c.4640+3G>T MANE Select | NP_001836.3:n.4640+3G>T |
| ENST00000375820.10:c.4640+3G>T MANE Select | ENSP00000364979.4:n.4640+3G>T |
| NM_001845.5:c.4640+3G>T | NP_001836.3:n.4640+3G>T |
| ENST00000375820.8:c.4640+3G>T | ENSP00000364979.4:n.4640+3G>T |
| ENST00000467182.1:n.422G>T | |
| ENST00000649720.1:n.808+3G>T | |
| ENST00000650424.1:c.796+3G>T | |
| XM_011521048.1:c.4448+3G>T | XP_011519350.1:n.4448+3G>T |
| XM_011521048.2:c.4448+3G>T | XP_011519350.1:n.4448+3G>T |