Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99842094G= , CM000672.2:g.99842094G= | GRCh38 |
| NC_000010.10:g.101601851G= , CM000672.1:g.101601851G= | GRCh37 |
| NC_000010.9:g.101591841G= | NCBI36 |
| NG_011798.1:g.64389G= | |
| NG_011798.2:g.64497G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000392.5:c.3741+1G= MANE Select | NP_000383.2:n.3741+1G= |
| ENST00000647814.1:c.3741+1G= MANE Select | ENSP00000497274.1:n.3741+1G= |
| NM_000392.4:c.3741+1G= | NP_000383.1:n.3741+1G= |
| ENST00000370449.8:c.3741+1G= | ENSP00000359478.4:n.3741+1G= |
| XM_006717630.2:c.3045+1G= | XP_006717693.1:n.3045+1G= |
| XM_006717630.3:c.3045+1G= | XP_006717693.1:n.3045+1G= |
| XR_945604.1:n.3930+1G= | |
| XR_945604.3:n.3984+1G= | |
| XR_945605.1:n.3806-1705G= | |
| XR_945605.3:n.3858-1705G= |