Canonical Allele Identifier:
CA1283487478
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.120331998A= , CM000664.2:g.120331998A= | GRCh38 |
| NC_000002.11:g.121089574A= , CM000664.1:g.121089574A= | GRCh37 |
| NC_000002.10:g.120806044A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011512307.1:c.141+3192A= | XP_011510609.1:n.141+3192A= |