Canonical Allele Identifier:
CA2477593062
Community Standard Title: NC_000001.11:g.89100413G>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.89100413G>C , CM000663.2:g.89100413G>C | GRCh38 |
| NC_000001.10:g.89566096G>C , CM000663.1:g.89566096G>C | GRCh37 |
| NC_000001.9:g.89338684G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_947575.1:n.5298G>C | |
| XR_947575.2:n.5305G>C | |
| XR_947576.1:n.2288G>C | |
| XR_947576.2:n.2413G>C |