Canonical Allele Identifier:
CA1905920005
Gene:
Linked Data
dbSNP Id:
rs2503875
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43318601G>T , CM000672.2:g.43318601G>T | GRCh38 |
| NC_000010.10:g.43814049G>T , CM000672.1:g.43814049G>T | GRCh37 |
| NC_000010.9:g.43134055G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_945902.1:n.108+6G>T | ||
| XR_945902.2:n.198+6G>T |