Canonical Allele Identifier:
CA1283487529
Gene:
Linked Data
dbSNP Id:
rs1690913933
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.120332116T>C , CM000664.2:g.120332116T>C | GRCh38 |
| NC_000002.11:g.121089692T>C , CM000664.1:g.121089692T>C | GRCh37 |
| NC_000002.10:g.120806162T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011512307.1:c.141+3310T>C | XP_011510609.1:n.141+3310T>C |