Canonical Allele Identifier:
CA1300258839
Gene:
Linked Data
dbSNP Id:
rs1683152137
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.155870679T>C , CM000664.2:g.155870679T>C | GRCh38 |
| NC_000002.11:g.156727191T>C , CM000664.1:g.156727191T>C | GRCh37 |
| NC_000002.10:g.156435437T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923501.1:n.320-3492A>G | ||
| XR_001739749.1:n.331-29695A>G | ||
| XR_001739750.1:n.331-29695A>G | ||
| XR_001739751.1:n.331-29695A>G | ||
| XR_923501.2:n.331-3492A>G |