Canonical Allele Identifier:
CA1655539979
Gene:
Linked Data
dbSNP Id:
rs10782174
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.112813274G>T , CM000668.2:g.112813274G>T | GRCh38 |
| NC_000006.11:g.113134476G>T , CM000668.1:g.113134476G>T | GRCh37 |
| NC_000006.10:g.113241169G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_001744300.1:n.59+33488C>A | ||
| XR_001744301.1:n.63+33488C>A | ||
| XR_001744302.1:n.59+33488C>A | ||
| XR_001744303.1:n.59+33488C>A |