Canonical Allele Identifier:
CA1284431611
Gene:
Linked Data
dbSNP Id:
rs1678945444
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122368773C>T , CM000664.2:g.122368773C>T | GRCh38 |
| NC_000002.11:g.123126349C>T , CM000664.1:g.123126349C>T | GRCh37 |
| NC_000002.10:g.122842819C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923278.1:n.556-24190C>T | ||
| XR_001739684.1:n.556-24190C>T |