Canonical Allele Identifier:
CA1804794433
Gene:
Linked Data
dbSNP Id:
rs1810400901
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.97269783G>A , CM000670.2:g.97269783G>A | GRCh38 |
| NC_000008.10:g.98282011G>A , CM000670.1:g.98282011G>A | GRCh37 |
| NC_000008.9:g.98351187G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125390.1:n.471+149287C>T |