Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.96299179G= , CM000675.2:g.96299179G= | GRCh38 |
| NC_000013.10:g.96951433G= , CM000675.1:g.96951433G= | GRCh37 |
| NC_000013.9:g.95749434G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_153456.4:c.707+207610G= MANE Select | NP_703157.2:n.707+207610G= |
| ENST00000376705.4:c.707+207610G= MANE Select | ENSP00000365895.2:n.707+207610G= |
| NM_153456.3:c.707+207610G= | NP_703157.2:n.707+207610G= |
| ENST00000376705.3:c.707+207610G= | ENSP00000365895.2:n.707+207610G= |
| XM_011521073.1:c.707+207610G= | XP_011519375.1:n.707+207610G= |
| XM_011521076.1:c.708-39814G= | XP_011519378.1:n.708-39814G= |
| XM_011521076.2:c.708-39814G= | XP_011519378.1:n.708-39814G= |
| XM_017020543.2:c.708-189036G= | XP_016876032.1:n.708-189036G= |