Canonical Allele Identifier:
CA1618483022
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29860883A= , CM000668.2:g.29860883A= | GRCh38 |
| NC_000006.11:g.29828660A= , CM000668.1:g.29828660A= | GRCh37 |
| NC_000006.10:g.29936639A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647952.1:n.2063-3445T= |