Canonical Allele Identifier:
CA1029770005
Gene:
Linked Data
dbSNP Id:
rs1667991732
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.41534668G>C , CM000664.2:g.41534668G>C | GRCh38 |
| NC_000002.11:g.41761808G>C , CM000664.1:g.41761808G>C | GRCh37 |
| NC_000002.10:g.41615312G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_939996.1:n.181+3058C>G | ||
| XR_939997.1:n.146+3058C>G | ||
| XR_939997.2:n.9529+3058C>G |