Canonical Allele Identifier:
CA2014002160
Gene:
Linked Data
dbSNP Id:
rs10849432
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6276561C>A , CM000674.2:g.6276561C>A | GRCh38 |
| NC_000012.11:g.6385727C>A , CM000674.1:g.6385727C>A | GRCh37 |
| NC_000012.10:g.6255988C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_001748976.1:n.157+16538G>T | ||
| XR_001748977.1:n.157+16538G>T | ||
| XR_001748978.1:n.157+16538G>T | ||
| XR_001748979.1:n.157+16538G>T | ||
| XR_001748980.1:n.157+16538G>T |