Canonical Allele Identifier:
CA1913040869
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.58444842G>T , CM000672.2:g.58444842G>T | GRCh38 |
| NC_000010.10:g.60204602G>T , CM000672.1:g.60204602G>T | GRCh37 |
| NC_000010.9:g.59874608G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945981.1:n.356+9185G>T | ||
| XR_945982.1:n.356+9185G>T | ||
| XR_945983.1:n.356+9185G>T | ||
| XR_945984.1:n.112+10801G>T | ||
| XR_945985.1:n.73+8636G>T | ||
| XR_945986.1:n.356+9185G>T | ||
| XR_945981.2:n.360+9185G>T | ||
| XR_945982.2:n.360+9185G>T | ||
| XR_945983.2:n.360+9185G>T | ||
| XR_945984.2:n.116+10801G>T | ||
| XR_945985.2:n.73+8636G>T |