Canonical Allele Identifier:
CA2000590709
Gene:
Linked Data
dbSNP Id:
rs1866727216
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112166701A>C , CM000673.2:g.112166701A>C | GRCh38 |
| NC_000011.9:g.112037424A>C , CM000673.1:g.112037424A>C | GRCh37 |
| NC_000011.8:g.111542634A>C | NCBI36 |
| NG_028143.1:g.2417T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525987.5:n.320-3718A>C | ||
| ENST00000531744.5:c.315-3718A>C | ENSP00000456957.1:n.315-3718A>C | |
| ENST00000532699.1:c.315-3718A>C | ENSP00000456434.1:n.315-3718A>C |