Canonical Allele Identifier:
CA2269950699
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63498402A= , CM000679.2:g.63498402A= | GRCh38 |
| NC_000017.10:g.61575763A= , CM000679.1:g.61575763A= | GRCh37 |
| NC_000017.9:g.58929495A= | NCBI36 |
| NG_011648.1:g.26330A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000577647.2:c.1969+1417A= | ENSP00000464149.1:n.1969+1417A= |