Canonical Allele Identifier:
CA2330336338
Gene:
Linked Data
dbSNP Id:
rs2011165234
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.28544771C>T , CM000681.2:g.28544771C>T | GRCh38 |
| NC_000019.9:g.29035678C>T , CM000681.1:g.29035678C>T | GRCh37 |
| NC_000019.8:g.33727518C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110759.1:n.657-77991G>A | ||
| XR_243979.1:n.110-51748G>A |