Canonical Allele Identifier:
CA2751927279
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.120331877G>T , CM000664.2:g.120331877G>T | GRCh38 |
| NC_000002.11:g.121089453G>T , CM000664.1:g.121089453G>T | GRCh37 |
| NC_000002.10:g.120805923G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011512307.1:c.141+3071G>T | XP_011510609.1:n.141+3071G>T |