Canonical Allele Identifier:
CA1818161745
Gene:
Linked Data
dbSNP Id:
rs1902432
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127012566A>T , CM000670.2:g.127012566A>T | GRCh38 |
| NC_000008.10:g.128024811A>T , CM000670.1:g.128024811A>T | GRCh37 |
| NC_000008.9:g.128093993A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_001746076.2:n.1364+5948A>T |