Canonical Allele Identifier:
CA2346213818
Gene:
Linked Data
dbSNP Id:
rs2087099843
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.2674203C>T , CM000682.2:g.2674203C>T | GRCh38 |
| NC_000020.10:g.2654849C>T , CM000682.1:g.2654849C>T | GRCh37 |
| NC_000020.9:g.2602849C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_937210.1:n.675-3763G>A | ||
| XR_937211.1:n.674-3620G>A | ||
| XR_937210.2:n.668-3763G>A | ||
| XR_937211.2:n.666-3620G>A |