Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.30736442G= , CM000675.2:g.30736442G= | GRCh38 |
| NC_000013.10:g.31310579G= , CM000675.1:g.31310579G= | GRCh37 |
| NC_000013.9:g.30208579G= | NCBI36 |
| NG_011963.2:g.27965G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001629.4:c.70+767G= MANE Select | NP_001620.2:n.70+767G= |
| ENST00000380490.5:c.70+767G= MANE Select | ENSP00000369858.3:n.70+767G= |
| NM_001204406.1:c.241+767G= | NP_001191335.1:n.241+767G= |
| NM_001204406.2:c.241+767G= | NP_001191335.1:n.241+767G= |
| NM_001629.3:c.70+767G= | NP_001620.2:n.70+767G= |
| ENST00000380490.4:c.70+767G= | ENSP00000369858.3:n.70+767G= |
| ENST00000617770.4:c.241+767G= | ENSP00000479870.1:n.241+767G= |
| XM_011535024.1:c.70+767G= | XP_011533326.1:n.70+767G= |