Canonical Allele Identifier:
CA2581880406
Community Standard Title: NC_000003.12:g.61428140C>T
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.61428140C>T , CM000665.2:g.61428140C>T | GRCh38 |
| NC_000003.11:g.61413814C>T , CM000665.1:g.61413814C>T | GRCh37 |
| NC_000003.10:g.61388854C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001740725.1:n.202+374G>A | |
| XR_940892.1:n.164+374G>A | |
| XR_940892.2:n.202+374G>A | |
| XR_940893.1:n.164+374G>A |