Canonical Allele Identifier:
CA11098119
Community Standard Title: NC_000002.12:g.218216574T>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218216574T>C , CM000664.2:g.218216574T>C | GRCh38 |
| NC_000002.11:g.219081297T>C , CM000664.1:g.219081297T>C | GRCh37 |
| NC_000002.10:g.218789542T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_241416.2:n.371A>G | |
| XR_923908.1:n.368A>G |