Canonical Allele Identifier:
CA1216113173
Gene:
Linked Data
dbSNP Id:
rs1435176788
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193121842G>C , CM000663.2:g.193121842G>C | GRCh38 |
| NC_000001.10:g.193090972G>C , CM000663.1:g.193090972G>C | GRCh37 |
| NC_000001.9:g.191357595G>C | NCBI36 |
| NG_012691.1:g.4885G>C , LRG_507:g.4885G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001738350.1:n.1815C>G |