Canonical Allele Identifier:
CA1880834443
Gene:
Linked Data
dbSNP Id:
rs1829779307
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129576891G>T , CM000671.2:g.129576891G>T | GRCh38 |
| NC_000009.11:g.132339170G>T , CM000671.1:g.132339170G>T | GRCh37 |
| NC_000009.10:g.131378991G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930390.1:n.182+1293G>T |