Linked Data
dbSNP Id:
rs1696533411
gnomAD v3:
2-214810235-C-G
MyVariant Identifiers:
chr2:g.215674959C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214810235C>G , CM000664.2:g.214810235C>G | GRCh38 |
| NC_000002.11:g.215674959C>G , CM000664.1:g.215674959C>G | GRCh37 |
| NC_000002.10:g.215383204C>G | NCBI36 |
| NG_012047.2:g.4470G>C | |
| NG_012047.3:g.4477G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110292.1:n.7C>G |