Canonical Allele Identifier:
CA2700867735
Gene:
Linked Data
dbSNP Id:
rs2105325475
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.155870523C>T , CM000664.2:g.155870523C>T | GRCh38 |
| NC_000002.11:g.156727035C>T , CM000664.1:g.156727035C>T | GRCh37 |
| NC_000002.10:g.156435281C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923501.1:n.320-3336G>A | ||
| XR_001739749.1:n.331-29539G>A | ||
| XR_001739750.1:n.331-29539G>A | ||
| XR_001739751.1:n.331-29539G>A | ||
| XR_923501.2:n.331-3336G>A |