Canonical Allele Identifier:
CA12229859
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29874690T>A , CM000668.2:g.29874690T>A | GRCh38 |
| NC_000006.11:g.29842467T>A , CM000668.1:g.29842467T>A | GRCh37 |
| NC_000006.10:g.29950446T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647952.1:n.2062+8864A>T |