Canonical Allele Identifier:
CA16091755
Community Standard Title: NC_000002.12:g.21617221C>T
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21617221C>T , CM000664.2:g.21617221C>T | GRCh38 |
| NC_000002.11:g.21840093C>T , CM000664.1:g.21840093C>T | GRCh37 |
| NC_000002.10:g.21693598C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001739327.1:n.2811-9311G>A | |
| XR_939810.1:n.2647-9311G>A |