Canonical Allele Identifier:
CA1438624484
Gene:
Linked Data
dbSNP Id:
rs1713318020
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.11501903G>T , CM000666.2:g.11501903G>T | GRCh38 |
| NC_000004.11:g.11503527G>T , CM000666.1:g.11503527G>T | GRCh37 |
| NC_000004.10:g.11112625G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741361.1:n.950+19057G>T |