Canonical Allele Identifier:
CA2065107396
Gene:
Linked Data
dbSNP Id:
rs1292011
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.115398717A>T , CM000674.2:g.115398717A>T | GRCh38 |
| NC_000012.11:g.115836522A>T , CM000674.1:g.115836522A>T | GRCh37 |
| NC_000012.10:g.114320905A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_945389.1:n.697+8378T>A | ||
| XR_945389.2:n.701+8378T>A |