Canonical Allele Identifier:
CA11405231
Community Standard Title: NC_000003.12:g.53057148C>T
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.53057148C>T , CM000665.2:g.53057148C>T | GRCh38 |
| NC_000003.11:g.53091164C>T , CM000665.1:g.53091164C>T | GRCh37 |
| NC_000003.10:g.53066204C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000607203.1:c.318-9909G>A | |
| ENST00000607283.5:c.465-13894G>A | |
| ENST00000607495.5:c.447+20540G>A |