Canonical Allele Identifier:
CA1163450887
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.38158632G= , CM000663.2:g.38158632G= | GRCh38 |
| NC_000001.10:g.38624304G= , CM000663.1:g.38624304G= | GRCh37 |
| NC_000001.9:g.38396891G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_947202.1:n.45-3061G= | ||
| XR_947203.1:n.61+16918G= | ||
| XR_947204.1:n.45-3061G= | ||
| XR_947205.1:n.45-3061G= | ||
| XR_001737984.1:n.45-3061G= | ||
| XR_001737985.1:n.61+16918G= | ||
| XR_001737986.1:n.45-3061G= | ||
| XR_001737987.1:n.45-3061G= | ||
| XR_002958294.1:n.45-3061G= | ||
| XR_947205.2:n.45-3061G= |