Canonical Allele Identifier:
CA1963376004
Gene:
Linked Data
dbSNP Id:
rs1851018040
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.34759401_34759405del , CM000673.2:g.34759401_34759405del | GRCh38 |
| NC_000011.9:g.34780948_34780952del , CM000673.1:g.34780948_34780952del | GRCh37 |
| NC_000011.8:g.34737524_34737528del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_428897.2:n.579+4794_579+4798del | ||
| XR_931188.1:n.693+4794_693+4798del | ||
| XR_931189.1:n.854+4794_854+4798del | ||
| XR_931190.1:n.639+4794_639+4798del | ||
| XR_931191.1:n.689+4794_689+4798del | ||
| XR_001748174.1:n.855+4794_855+4798del | ||
| XR_001748176.1:n.1016+4794_1016+4798del | ||
| XR_002957246.1:n.639+4794_639+4798del |