Canonical Allele Identifier:
CA1823425143
Community Standard Title: NC_000008.11:g.137906702C=
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.137906702C= , CM000670.2:g.137906702C= | GRCh38 |
| NC_000008.10:g.138918945C= , CM000670.1:g.138918945C= | GRCh37 |
| NC_000008.9:g.138988127C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001354876.1:c.250-68817G= | NP_001341805.1:n.250-68817G= |
| NR_161374.1:n.574-68817G= | |
| XM_024447147.1:c.334-68817G= | XP_024302915.1:n.334-68817G= |
| XM_024447148.1:c.334-68817G= | XP_024302916.1:n.334-68817G= |
| XM_024447149.1:c.250-68817G= | XP_024302917.1:n.250-68817G= |
| XM_024447150.1:c.136-68817G= | XP_024302918.1:n.136-68817G= |
| XM_024447151.1:c.334-68817G= | XP_024302919.1:n.334-68817G= |
| XR_928696.1:n.985+33024G= | |
| XR_928697.1:n.574-68817G= |