Canonical Allele Identifier:
CA315556725
Gene:
MyVariant.info:
GRCh38
chr20:g.45495883A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.45495883A>T , CM000682.2:g.45495883A>T | GRCh38 |
| NC_000020.10:g.44124523A>T , CM000682.1:g.44124523A>T | GRCh37 |
| NC_000020.9:g.43557937A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001754641.2:n.67+8173A>T |