Canonical Allele Identifier:
CA1391023728
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.106193283T>A , CM000665.2:g.106193283T>A | GRCh38 |
| NC_000003.11:g.105912130T>A , CM000665.1:g.105912130T>A | GRCh37 |
| NC_000003.10:g.107394820T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_924311.1:n.176-517T>A | ||
| XR_924312.1:n.176-9231T>A | ||
| XR_924311.2:n.176-517T>A |