Canonical Allele Identifier:
CA799758167
Gene:
Linked Data
dbSNP Id:
rs928316228
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89597813G>T , CM000666.2:g.89597813G>T | GRCh38 |
| NC_000004.11:g.90518964G>T , CM000666.1:g.90518964G>T | GRCh37 |
| NC_000004.10:g.90737987G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.298+9873G>T | ||
| XR_938987.1:n.433-340G>T | ||
| XR_938988.1:n.299-340G>T | ||
| XR_938990.1:n.298+9873G>T | ||
| XR_938991.1:n.298+9873G>T | ||
| XR_938992.1:n.298+9873G>T | ||
| XR_938994.1:n.643+9873G>T | ||
| XR_938995.1:n.477+9873G>T | ||
| XR_938996.1:n.298+9873G>T | ||
| XR_938997.1:n.298+9873G>T | ||
| XR_938986.2:n.323+9873G>T | ||
| XR_938987.2:n.493-340G>T |