Canonical Allele Identifier:
CA1941455994
Gene:
Linked Data
dbSNP Id:
rs2097478761
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122458359A>T , CM000672.2:g.122458359A>T | GRCh38 |
| NC_000010.10:g.124217875A>T , CM000672.1:g.124217875A>T | GRCh37 |
| NC_000010.9:g.124207865A>T | NCBI36 |
| NG_011554.1:g.1835A>T | |
| NG_011725.1:g.8697A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_946382.1:n.1827+136T>A | ||
| XR_946383.1:n.1827+136T>A | ||
| XR_946384.1:n.1576+136T>A | ||
| XR_946385.1:n.1827+136T>A | ||
| XR_946382.2:n.1855+136T>A | ||
| XR_946383.2:n.1855+136T>A | ||
| XR_946384.2:n.1580+136T>A | ||
| XR_946385.2:n.1855+136T>A |