Canonical Allele Identifier:
CA2346122826
Gene:
Linked Data
dbSNP Id:
rs2085112682
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.2471027A>T , CM000682.2:g.2471027A>T | GRCh38 |
| NC_000020.10:g.2451673A>T , CM000682.1:g.2451673A>T | GRCh37 |
| NC_000020.9:g.2399673A>T | NCBI36 |
| NG_042057.1:g.4827T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461548.1:c.305-3269T>A | ENSP00000456213.1:n.305-3269T>A |