Canonical Allele Identifier:
CA2553159069
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128455410T>C , CM000673.2:g.128455410T>C | GRCh38 |
| NC_000011.9:g.128325305T>C , CM000673.1:g.128325305T>C | GRCh37 |
| NC_000011.8:g.127830515T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948164.1:n.4130T>C | ||
| XR_948165.1:n.3467+663T>C |